Aymé-Gripp syndrome

Orpha code: 1272OMIM code: 601353

Definition

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by congenital cataract, sensorineural hearing loss, developmental delay with variable degrees of intellectual disability, seizures, short stature, brachycephaly, and dysmorphic facial features (such as flat facial appearance, ptosis, short nasal tip, long philtrum, low-set and posteriorly rotated ears, and small mouth). Additional reported manifestations are skeletal abnormalities, nail dystrophy, mammary gland hypoplasia, and autism spectrum disorder.

Disease data
Classification

Malformation syndrome

Synonyms
Brachycephaly-deafness-cataract-intellectual disability syndrome
Krótkogłowie - głuchota - zaćma - niepełnosprawność intelektualna
Brachycephaly-hearing loss-cataract-intellectual disability syndrome
Fine-Lubinsky syndrome
ORPHA code
1272
OMIM code
601353
ICD10 code
Q87.8
ICD11 code
-

No additional description.

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