Aymé-Gripp syndrome

Disease Export to PDF
Name:
Aymé-Gripp syndrome
Description:
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.
ORPHAcode:
1272
Synonyms:
Brachycephaly-deafness-cataract-intellectual disability syndrome
Brachycephaly-hearing loss-cataract-intellectual disability syndrome
Fine-Lubinsky syndrome
XREF(s):
Analyte(s):
Created:
20 Aug 2021 - 01:14
Changed:
22 Jun 2023 - 16:14