TERMIUM Plus^®

Record 1,  Textual support,  English

Record number: 1, Textual support number: 1 CONT

Ivemark syndrome is a rare disorder that affects multiple organ systems of the body. It is characterized by the absence(asplenia) or underdevelopment(hypoplasia) of the spleen, malformations of the heart and the abnormal arrangement of the internal organs of the chest and abdomen.  3, record 1, English, - Ivemark%20syndrome

Record 1,  Textual support,  French

Record number: 1, Textual support number: 1 OBS

L'asplénie congénitale peut être observée soit de façon isolée ou soit associée dans un syndrome malformatif, comme dans le syndrome d'Ivemark.  2, record 1, French, - syndrome%20d%27Ivemark

Record 1,  Textual support,  Spanish

Record 2,  Textual support,  English

Record number: 2, Textual support number: 1 CONT

Joubert syndrome(JS) and related disorders are a group of autosomal-recessive conditions sharing the "molar tooth sign" on axial brain MRI [magnetic resonance imaging], together with cerebellar vermis hypoplasia, ataxia, and psychomotor delay. JS is suggested to be a disorder of cilia function and is part of a spectrum of disorders involving retinal, renal, digital, oral, hepatic, and cerebral organs.  3, record 2, English, - Joubert%20syndrome

Record 2,  Textual support,  French

Record number: 2, Textual support number: 1 DEF

Syndrome d'hérédité autosomique récessive [...] caractérisé par une malformation congénitale du tronc cérébral et une agénésie ou une hypoplasie du vermis cérébelleux entraînant des troubles respiratoires, un nystagmus, une hypotonie, une ataxie et un retard du développement moteur.  2, record 2, French, - syndrome%20de%20Joubert

Record 2,  Textual support,  Spanish

Record 3,  Textual support,  English

Record number: 3, Textual support number: 1 DEF

The complete form of a hereditary disorder which is called mandibulofacial dysostosis. The Franceschetti syndrome is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal dominant trait.  1, record 3, English, - Franceschetti%26rsquo%3Bs%20disease

Record number: 3, Textual support number: 1 CONT

(Trisomy 18) Finally, the small lower jaw gives a receding chin suggestive of Franceschetti’s disease.  1, record 3, English, - Franceschetti%26rsquo%3Bs%20disease

Record 3,  Textual support,  French

Record number: 3, Textual support number: 1 DEF

Affection du fond d'œil se caractérisant par la présence, au niveau ou autour du pôle postérieur (parfois à la périphérie), de taches jaunes situées dans les couches profondes de la rétine, disséminées ou groupées en grappe, de forme variable (arrondie, allongée, ou étoilée).  1, record 3, French, - maladie%20de%20Franceschetti

Record number: 3, Textual support number: 1 CONT

(Trisomie 18) Enfin, la mâchoire inférieure est petite, le menton nettement en retrait sur le massif facial donnant un aspect pouvant rappeler la maladie de Franceschetti.  1, record 3, French, - maladie%20de%20Franceschetti

Record 3,  Textual support,  Spanish

Record 4,  Textual support,  English

Record number: 4, Textual support number: 1 CONT

CHARGE syndrome is a multiple congenital anomaly syndrome. The acronym CHARGE is based on cardinal features identified when the syndrome was first delineated-coloboma, congenital heart defects, choanal atresia, retardation of growth, developmental delay, genital abnormalities, ear abnormalities and deafness. A consistent feature of CHARGE syndrome is semicircular canal hypoplasia resulting in vestibular areflexia. Neonates with CHARGE syndrome often have multiple life-threatening medical conditions.  2, record 4, English, - CHARGE%20syndrome

Record 4,  Textual support,  French

Record number: 4, Textual support number: 1 CONT

Le syndrome CHARGE est une maladie rare qui affecte différentes parties du corps. Il est à présent reconnu comme étant la cause majeure de la surdité et cécité congénitale. Le terme « CHARGE » est un acronyme des critères majeurs de cette maladie.  4, record 4, French, - syndrome%20CHARGE

Record number: 4, Textual support number: 2 CONT

L'acronyme CHARGE désigne un ensemble de malformations congénitales comprenant un colobome, une cardiopathie, une atrésie des choanes, un retard statural et de développement, une hypoplasie génitale et une anomalie des oreilles. Plusieurs arguments sont en faveur d'une origine génétique dans ce syndrome, en particulier une concordance clinique observée chez les jumeaux monozygotes.  5, record 4, French, - syndrome%20CHARGE

Record 4,  Textual support,  Spanish

Record 5,  Textual support,  English

Record number: 5, Textual support number: 1 DEF

Pertaining to hypoplasia or the incomplete development of a tissue or organ.  2, record 5, English, - hypoplastic

Record number: 5, Textual support number: 1 CONT

The hypoplastic lymphatics lead to an obstruction in lymph flow, increased pressure within lymphatics, dilated lymphatic channels in the intestine, and finally rupture of the lymphatic channels, discharging lymph into the bowel lumen.  1, record 5, English, - hypoplastic

Record 5,  Textual support,  French

Record number: 5, Textual support number: 1 DEF

Relatif à l'hypoplasie (développement incomplet d'un tissu ou d'un organe).  2, record 5, French, - hypoplasique

Record number: 5, Textual support number: 1 CONT

Rein hypoplasique.  1, record 5, French, - hypoplasique

Record 5,  Textual support,  Spanish

Record number: 5, Textual support number: 1 DEF

[Dícese del] crecimiento o desarrollo defectivo y reducido [...] resultado de una condición anómala, por ejemplo enfermedad o estrés nutricional.  1, record 5, Spanish, - hipopl%C3%A1stico

Record 6,  Textual support,  English

Record number: 6, Textual support number: 1 DEF

A condition characterized by hypoplasia of the extremities of the skeleton-the nose, jaws, fingers, and toes; the converse of acromegaly.  1, record 6, English, - acromicria

Record 6,  Textual support,  French

Record number: 6, Textual support number: 1 DEF

Syndrome décrit par Brugsch, caractérisé par un nanisme micromélique, avec infantilisme des organes génitaux, surtout chez la femme, mais sans déficience de la libido, et par l'adiposité de la tête et du tronc.  1, record 6, French, - acromicrie

Record 6,  Textual support,  Spanish

Record 7,  Textual support,  English

Record number: 7, Textual support number: 1 OBS

hypotrophy, hypoplasia : underdevelopment, undernourishment.  3, record 7, English, - hypotrophic%20uterus

Record 7,  Textual support,  French

Record number: 7, Textual support number: 1 DEF

Utérus insuffisamment développé.  1, record 7, French, - ut%C3%A9rus%20hypotrophique

Record 7,  Textual support,  Spanish

Record 8,  Textual support,  English

Record number: 8, Textual support number: 1 DEF

A hereditary disorder occurring in two forms : the complete form(Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an auto-somal dominant trait. The incomplete form(Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected.  2, record 8, English, - mandibulofacial%20dysostosis

Record number: 8, Textual support number: 1 CONT

The syndrome ... consists of certain associated congenital and familial deformities of the ears, malar bones, lips, chin and lower eyelids.... There may be microtia, meatal atresia and auricular fistulae. Malformation of the middle and inner ear produces conductive or perceptive deafness....  3, record 8, English, - mandibulofacial%20dysostosis

Record 8,  Textual support,  French

Record number: 8, Textual support number: 1 DEF

[...] maladie héréditaire dominante, avec anomalies de la face, de la bouche et des oreilles, due à une hypoplasie osseuse qui porte surtout sur les os malaires (pommettes).  1, record 8, French, - dysostose%20mandibulo%2Dfaciale

Record number: 8, Textual support number: 1 OBS

Le nez paraît important en raison de l'hypoplasie de l'étage moyen mais les narines sont étroites et les cartilages alaires, hypoplasiques. La bouche est trop grande et des fissures borgnes s'ouvrent entre les commissures et les oreilles. Les dents sont mal plantées, une division palatine est fréquente. La micrognathie est constante et importante. Le pavillon de l'oreille est malformé, hypoplasique avec une atrésie du canal auditif, des appendices et fistules pré-auriculaires. Ces anomalies s'accompagnent d'altérations des osselets responsables d'une surdité de conduction. [...] La transmission est dominante autosomique à expression très variable.  2, record 8, French, - dysostose%20mandibulo%2Dfaciale

Record 8,  Textual support,  Spanish

Record 9,  Textual support,  English

Record number: 9, Textual support number: 1 DEF

Incomplete development or underdevelopment of an organ or tissue; it is less severe than aplasia.  2, record 9, English, - hypoplasia

Record number: 9, Textual support number: 1 OBS

In the musculoskeletal system, it may be failure of a bone to grow to a normal size.  3, record 9, English, - hypoplasia

Record 9,  Textual support,  French

Record number: 9, Textual support number: 1 DEF

Développement incomplet d'un tissu ou d'un organe.  2, record 9, French, - hypoplasie

Record 9,  Textual support,  Spanish

Record number: 9, Textual support number: 1 DEF

Reducción anormal del número de células de los tejidos que conduce a la atrofia de un órgano.  3, record 9, Spanish, - hipoplasia

Record 10,  Textual support,  English

Record number: 10, Textual support number: 1 DEF

A congenital hypoplastic anemia that occurs especially in early infancy; it is, in general, characterized by a moderate-to-severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular bone marrow with erythroid hypoplasia, and an increased risk of developing leukemia.  1, record 10, English, - Blackfan%20and%20Diamond%20anemia

Record 10,  Textual support,  French

Record number: 10, Textual support number: 1 DEF

Anémie chronique normochrome, normocytaire, arégénérative, survenant dans les premiers mois de la vie, due à une érythrogénèse imparfaite et qui, en général, se manifeste par une forte anémie, une réticulocytopénie absolue et une érythroblastopénie médullaire ou un blocage de la maturation des érythroblastes.  1, record 10, French, - an%C3%A9mie%20de%20Blackfan%2DDiamond

Record number: 10, Textual support number: 1 OBS

anémie hypoplastique congénitale : synonyme attesté mais discutable.  1, record 10, French, - an%C3%A9mie%20de%20Blackfan%2DDiamond

Record 10,  Textual support,  Spanish

Record 11,  Textual support,  English

Record number: 11, Textual support number: 1 DEF

An autosomal dominant or X-linked disorder in which there isfaulty development of the dental enamel owing to agenesis, hypoplasia, or hypocalcification of the enamel. It is marked by enamel that is very thin and friable and frequently stained in various shades of brown.  1, record 11, English, - amelogenesis%20imperfecta

Record 11,  Textual support,  French

Record number: 11, Textual support number: 1 CONT

Les dyschromies intrinsèques sur les dents pulpées peuvent avoir : des étiologies héréditaires (dentinogénèse ou amélogénèse imparfaites) [...]  1, record 11, French, - am%C3%A9log%C3%A9n%C3%A8se%20imparfaite

Record 11,  Textual support,  Spanish

Record 12,  Textual support,  English

Record number: 12, Textual support number: 1 DEF

One of the rarest anomalies of the hand characterized by a strongly flexed thumb across the palm of the hand as a result of developmental deficiency of the extensor mechanism of the thumb.  2, record 12, English, - congenital%20clasped%20thumb

Record number: 12, Textual support number: 1 OBS

The condition must be differentiated from spastic thumb-clutched deformity of cerebral palsy, which is due to spasticity of the adductor pollicis. The latter condition discloses diminution of deformity by passively flexing the wrist and intact thumb extensors evidenced by electromyographic studies.  3, record 12, English, - congenital%20clasped%20thumb

Record number: 12, Textual support number: 2 OBS

Definition from The Genetics of Hand Malformations, 1978, p. 445 and Orthopaedics: Principles and their Application, 1984, p. 290.  4, record 12, English, - congenital%20clasped%20thumb

Record 12,  Textual support,  French

Record number: 12, Textual support number: 1 DEF

Malformation rare du pouce caractérisée par la flexion permanente de la métacarpophalangienne et due à une anomalie (hypoplasie ou absence) du muscle court extenseur du pouce.  2, record 12, French, - pouce%20flexus%2Dadductus%20cong%C3%A9nital

Record number: 12, Textual support number: 1 OBS

Définition d'après l'Encyclopédie médico-chirurgicale : appareil locomoteur, s.d., p. 2.  3, record 12, French, - pouce%20flexus%2Dadductus%20cong%C3%A9nital

Record 12,  Textual support,  Spanish

Record number: 12, Textual support number: 1 OBS

Término formado a partir de la fuente Diccionari Enciclopèdic de Medicina, Barcelona: Fundació Enciclopèdia Catalana, 1990.  1, record 12, Spanish, - pulgar%20r%C3%ADgido

Record 13,  Textual support,  English

Record number: 13, Textual support number: 1 DEF

A rare recessive disorder with a poor prognosis, characterized by pancytopenia, bone marrow hypoplasia, and patchy brown skin discoloration due to deposition of melanin, as well as multiple congenital anomalies of the musculoskeletal and genitourinary systems.  1, record 13, English, - Fanconi%26rsquo%3Bs%20syndrome

Record 13,  Textual support,  French

Record number: 13, Textual support number: 1 DEF

Affection rare, de transmission héréditaire autosomique récessive, dont les symptômes chez les patients homozygotes associent des malformations congénitales du squelette (anomalies hexadactyles), des reins (fusionnés en fer à cheval), la présence de taches pigmentées sur la peau et surtout une pancytopénie progressive, par insuffisance de production de la moelle osseuse apparaissant au cours de la première décennie de la vie.  1, record 13, French, - maladie%20de%20Fanconi

Record 13,  Textual support,  Spanish

Record 14,  Textual support,  English

Record number: 14, Textual support number: 1 DEF

Abnormal smallness of the mamma.  7, record 14, English, - micromastia

Record 14,  Textual support,  French

Record number: 14, Textual support number: 1 DEF

Petitesse anormale des seins.  1, record 14, French, - micromastie

Record 14,  Textual support,  Spanish

Record number: 14, Textual support number: 1 DEF

Falta de desarrollo de una o ambas mamas.  3, record 14, Spanish, - micromastia

Record number: 14, Textual support number: 1 CONT

La micromastia (o hipomastia) es el desarrollo imperfecto de las mamas que da lugar a unas mamas de tamaño menor al que corresponde a una mujer adulta. Suele acompañarse de deformaciones mamarias.  2, record 14, Spanish, - micromastia

Record 15,  Textual support,  English

Record number: 15, Textual support number: 1 OBS

adenohypophyseal: Of, or relating to the adenohypophysis.  2, record 15, English, - adenohypophyseal%20hypoplasia

Record number: 15, Textual support number: 2 OBS

adenohypophysis: The portion of the pituitary body that arises from the embryonic pharynx and is predomimantly glandular in nature.  3, record 15, English, - adenohypophyseal%20hypoplasia

Record number: 15, Textual support number: 3 OBS

hypoplasia : Under-development.  4, record 15, English, - adenohypophyseal%20hypoplasia

Record 15,  Textual support,  French

Record number: 15, Textual support number: 1 OBS

adéno-hypophysaire : qui se rapporte à l'adénohypophyse.  2, record 15, French, - hypoplasie%20ad%C3%A9no%2Dhypophyaire

Record number: 15, Textual support number: 2 OBS

adénohypophyse : partie endocrinienne de l'hypophyse [...] qui appartient au cerveau (synonyme lobe antérieur de l'hypophyse.)  3, record 15, French, - hypoplasie%20ad%C3%A9no%2Dhypophyaire

Record 15,  Textual support,  Spanish

Record 16,  Textual support,  English

Record number: 16, Textual support number: 1 DEF

Gross hypoplasia or aplasia of the pinna of the ear, with a blind or absent external auditory meatus.  2, record 16, English, - microtia

Record 16,  Textual support,  French

Record number: 16, Textual support number: 1 DEF

Aplasie totale ou partielle, unie ou bilatérale du pavillon de l'oreille, avec ou sans atteinte du conduit auditif.  2, record 16, French, - microtie

Record 16,  Textual support,  Spanish

Record 17,  Textual support,  English

Record number: 17, Textual support number: 1 DEF

A hereditary defect of enamel matrix formation, with deficiency of enamel rods and cementing substance; enamel is hard but thin, teeth may be conical or cylindrical shape, with lack of contact between teeth, occlusal surfaces become worn, and yellow staining appears where the dentin is exposed; both deciduous and permanent teeth are affected. A type of amelogenesis imperfecta.  2, record 17, English, - enamel%20hypoplasia

Record 17,  Textual support,  French

Record 17,  Textual support,  Spanish

Record 18,  Textual support,  English

Record number: 18, Textual support number: 1 CONT

The eligible expenses incurred for such contact lenses, telescopic lenses or other subnormal vision aids.  1, record 18, English, - subnormal%20vision%20aid

Record number: 18, Textual support number: 2 CONT

Recognition of subtle forms and segmental forms of optic nerve hypoplasia are important in explaining the evaluation of subnormal vision, and have an added significance in the recognised associations of central nervous system anomalies including abnormalities of the endocrine system.  2, record 18, English, - subnormal%20vision%20aid

Record 18,  Textual support,  French

Record number: 18, Textual support number: 1 OBS

Les auteurs étudient 73 enfants. Chez 34,2%, la principale cause de vision subnormale est la choriorétinite.  1, record 18, French, - proth%C3%A8se%20pour%20vision%20subnormale

Record 18,  Textual support,  Spanish

Record 19,  Textual support,  English

Record number: 19, Textual support number: 1 DEF

A congenital defect of the hindlimbs of piglets that prevents standing.  2, record 19, English, - spraddleleg

Record number: 19, Textual support number: 1 OBS

The piglet is in sternal recumbency with the hindlimbs splayed and can only make swimming movements in attempts to rise.  2, record 19, English, - spraddleleg

Record 19,  Textual support,  French

Record number: 19, Textual support number: 1 DEF

Affection du porc se manifestant par une anomalie des fibrilles musculaires.  1, record 19, French, - hypoplasie%20myofibrillaire

Record 19,  Textual support,  Spanish

Record 20,  Textual support,  English

Record number: 20, Textual support number: 1 DEF

... disorder attributable to congenital aplasia or hypoplasia of the thymus that leads to cellular immunity dysfunction. It is also associated with abnormalities of the parathyroid glands and with consequent hypo-calcemic tetany and congenital heart disease. The diagnosis is suspected by neonatal hypocalcemia and chronic infection with various viral, fungal, protozoal, or bacterial organisms. The chest roentgenogram usually shows absence of the thymus.  1, record 20, English, - Di%20George%20syndrome

Record 20,  Textual support,  French

Record number: 20, Textual support number: 1 DEF

Déficit prédominant de l'immunité cellulaire. Absence congénitale de thymus et de parathyroïdes. C'est une embryopathie liée à une anomalie du développement des 3e et 4e arcs branchiaux. [...] L'aplasie thymique est caractérisée du point de vue immunologique par une absence complète des fonctions, T, analogue à celle provoquée par la thymectomie néonatale chez la souris. Les cellules T étudiées par leurs différents marqueurs ne sont pas détectables dans le sang périphérique ni dans les zones thymo-dépendantes paracorticales des ganglions [...]  1, record 20, French, - syndrome%20de%20Di%20George

Record 20,  Textual support,  Spanish

Record 21,  Textual support,  English

Record number: 21, Textual support number: 1 DEF

Congenital dislocation of the hip consisting of laterad and cephalad shifts of the femoral head, hypoplasia or absence of the femoral ossification center, and increased declivity of the acetabular roof toward the longitudinal axis of the body.  1, record 21, English, - Putti%26rsquo%3Bs%20triad

Record 21,  Textual support,  French

Record number: 21, Textual support number: 1 DEF

Luxation congénitale de la hanche se traduisant par le déplacement de la tête fémorale en haut et en dehors, une hypoplasie du noyau épiphysaire fémoral supérieur et une obliquité du toit du cotyle avec augmentation de l'angle acétabulaire. [D'après TRIAR, 1974, vol. 3, p. 205 et EMSQU, 31105, A10, 1984, p. 9.]  2, record 21, French, - triade%20de%20Putti

Record 21,  Textual support,  Spanish

Record 22,  Textual support,  English

Record number: 22, Textual support number: 1 DEF

Hypoplasia of the patella.  1, record 22, English, - patella%20parva

Record 22,  Textual support,  French

Record number: 22, Textual support number: 1 DEF

Hypoplasie rotulienne.  1, record 22, French, - patella%20parva

Record 22,  Textual support,  Spanish

Record 23,  Textual support,  English

Record number: 23, Textual support number: 1 DEF

Bony processes projecting dorsally from the outer surface of the wings of each ilium. They may occur alone or be associated with the syndrome of rudimentary or absent patellae, deformity of the elbows(hypoplasia of capitellum and radial head) and dystrophy of the nails(nail-patella syndrome). [From TEXRA, 1975, p. 9. ]  2, record 23, English, - iliac%20horns

Record 23,  Textual support,  French

Record number: 23, Textual support number: 1 DEF

Exostoses développées à la face externe de l'aile iliaque, observées notamment dans l'ostéonychodysostose. [D'après RACLI, 1974, vol. 3, p. 197.]  3, record 23, French, - cornes%20iliaques

Record 23,  Textual support,  Spanish

Record 24,  Textual support,  English

Record number: 24, Textual support number: 1 CONT

Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness. (In Archives of Ophthalmology, 1989, 107 (8) 1170-1179, cited in PASCAL data base.)  1, record 24, English, - Aland%20Island%20eye%20disease

Record number: 24, Textual support number: 2 CONT

Aland island eye disease(forsius-eriksson ocular albinism) and Xp21 deletion in a patient with duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia.(In American journal of medical genetics, 1990, 36(1) 23-28, cited in PASCAL data base.)  1, record 24, English, - Aland%20Island%20eye%20disease

Record 24,  Textual support,  French

Record number: 24, Textual support number: 1 CONT

Différents types d'albinisme - [...] Albinisme oculaire [...] Syndrome de Forsins-Eriksson - Maladie des yeux d'Aland (variété allélique ou pseudo-allélique du précédent)  1, record 24, French, - maladie%20des%20yeux%20d%27Aland

Record 24,  Textual support,  Spanish

Record 25,  Textual support,  English

Record number: 25, Textual support number: 1 CONT

We describe two females with de novo X;Y translocations, who presented at birth with irregular linear areas of erythematous skin hypoplasia involving the head and neck, along with eye findings that included microphthalmia, corneal opacities, and orbital cysts. Cytogenetic analysis has shown the X chromosome breakpoint in both females to be at Xp22. 3. We suggest that this syndrome is the result of a deletion or disruption of DNA sequences in the region of Xp22. 3.  2, record 25, English, - breakpoint

Record number: 25, Textual support number: 1 OBS

Tiré de: Journal of Medical Genetics, 1990, 27 (1), 59-63.  2, record 25, English, - breakpoint

Record 25,  Textual support,  French

Record number: 25, Textual support number: 1 CONT

La modification de l'expression de gènes intervenant dans le contrôle, positif ou négatif, de la prolifération cellulaire, et localisés à proximité des points de cassure, est probablement impliquée dans l'émergence des clones malins qui sont à l'origine de ces leucémies et lymphomes.  1, record 25, French, - point%20de%20cassure

Record 25,  Textual support,  Spanish

Record 26,  Textual support,  English

Record number: 26, Textual support number: 1 DEF

A congenital disorder, possibly due to various causes, characterized by low birth weight, marked but proportionate shortness of stature, a proportionately small head, hypoplasia of the maxilla and mandible with beak-like protrusion of the nose, mental retardation, and a variety of other skeletal, cutaneous and genital anomalies.  1, record 26, English, - bird%2Dheaded%20dwarfism

Record 26,  Textual support,  French

Record number: 26, Textual support number: 1 DEF

Variété rare du nanisme essentiel à début intra-utérin, caractérisée par une dysmorphie faciale particulière en "tête d'oiseau" (microcéphalie, hypoplasie des maxillaires, rétrognathisme, nez "en bec d'oiseau", implantation basse des oreilles). Il peut s'y associer des anomalies du palais, des dents, des doigts, et un retard mental.  1, record 26, French, - nanisme%20%C3%A0%20t%C3%AAte%20d%27oiseau

Record 26,  Textual support,  Spanish

Record 27,  Textual support,  English

Record number: 27, Textual support number: 1 DEF

Gross hypoplasia or aplasia of one of more long bones of one or more limbs....  1, record 27, English, - ectromelia

Record number: 27, Textual support number: 1 OBS

The term includes amelia, hemimelia and phocomelia.  1, record 27, English, - ectromelia

Record 27,  Textual support,  French

Record number: 27, Textual support number: 1 DEF

Défaut de développement total ou partiel d'un ou plusieurs membres ou segments de membre par agénésie squelettique.  1, record 27, French, - ectrom%C3%A9lie

Record number: 27, Textual support number: 1 OBS

L'ectromélie comprend l'amélie, l'hémimélie et la phocomélie.  2, record 27, French, - ectrom%C3%A9lie

Record 27,  Textual support,  Spanish

Record 28,  Textual support,  English

Record number: 28, Textual support number: 1 DEF

Hypoplasia of the patella.  2, record 28, English, - patella%20parva

Record 28,  Textual support,  French

Record number: 28, Textual support number: 1 DEF

Hypoplasie rotulienne.  2, record 28, French, - patella%20parva

Record 28,  Textual support,  Spanish

Record 29,  Textual support,  English

Record number: 29, Textual support number: 1 OBS

Flaccidity of the epiglottis and aryepiglottic folds, as in congenital laryngeal stridor.  1, record 29, English, - laryngomalacia

Record number: 29, Textual support number: 2 OBS

(Deletion of half the short arm of 5(Cri du chat syndrome)) This latter sign, extremely typical in the first month of life, seems to be related to a supraglottal hypoplasia with laryngomalacia.  1, record 29, English, - laryngomalacia

Record number: 29, Textual support number: 3 OBS

The "Dictionnaire de médecine" (Flammarion) mentions "congenital stridor" as [a] translation for "laryngomalacie". In fact, it is a looseness. According to French authors chronic (or congenital) stridors of the new-born are subdivided into tracheal and laryngeal stridors, and 60% of the cases of laryngeal stridors are known as laryngomalacia.  1, record 29, English, - laryngomalacia

Record 29,  Textual support,  French

Record number: 29, Textual support number: 1 OBS

Affection congénitale caractérisée par l'apparition, dans les premiers jours de la vie, d'un bruit respiratoire, à type de cornage, variable et intermittent, souvent associé à des troubles de la déglutition, à des accès dyspnéiques parfois dramatiques et à d'autres anomalies.  1, record 29, French, - laryngomalacie

Record number: 29, Textual support number: 2 OBS

(Délétion du bras court de l'autosome 8) Cette laryngomalacie serait la cause du curieux stridor de ces petits patients.  1, record 29, French, - laryngomalacie

Record 29,  Textual support,  Spanish