Back to Search
Start Over
Skeletal abnormalities are common features in Aymé‐Gripp syndrome
- Source :
- Clinical Genetics. 97:362-369
- Publication Year :
- 2019
- Publisher :
- Wiley, 2019.
-
Abstract
- Aymé-Gripp syndrome (AYGRPS) is a recognizable condition caused by a restricted spectrum of dominantly acting missense mutations affecting the transcription factor MAF. Major clinical features of AYGRPS include congenital cataracts, sensorineural hearing loss, intellectual disability, and a distinctive flat facial appearance. Skeletal abnormalities have also been observed in affected individuals, even though these features have not been assessed systematically. Expanding the series with four additional patients, here we provide a more accurate delineation of the molecular aspects and clinical phenotype, particularly focusing on the skeletal features characterizing this disorder. Apart from previously reported malar flattening and joint limitations, we document that carpal/tarsal and long bone defects, and hip dysplasia occur in affected subjects more frequently than formerly appreciated.
- Subjects :
- Adult
Male
0301 basic medicine
medicine.medical_specialty
Adolescent
Hearing Loss, Sensorineural
Long bone
Mutation, Missense
bone defects
skeletal dysplasia
030105 genetics & heredity
Cataract
AYME-GRIPP SYNDROME
Young Adult
03 medical and health sciences
Intellectual Disability
Intellectual disability
Genetics
medicine
Humans
Missense mutation
Genetic Predisposition to Disease
Child
Growth Disorders
Genetics (clinical)
Hip dysplasia
MAF
Aymé-Gripp syndrome
business.industry
Facies
Infant
medicine.disease
Dermatology
Musculoskeletal Abnormalities
030104 developmental biology
medicine.anatomical_structure
Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA
Child, Preschool
Proto-Oncogene Proteins c-maf
Congenital cataracts
Female
Sensorineural hearing loss
Skeletal abnormalities
business
Subjects
Details
- ISSN :
- 13990004 and 00099163
- Volume :
- 97
- Database :
- OpenAIRE
- Journal :
- Clinical Genetics
- Accession number :
- edsair.doi.dedup.....cb6fc22cd7da3d1e14fef570eac08c00