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Skeletal abnormalities are common features in Aymé-Gripp syndrome.
- Source :
-
Clinical genetics [Clin Genet] 2020 Feb; Vol. 97 (2), pp. 362-369. Date of Electronic Publication: 2019 Nov 03. - Publication Year :
- 2020
-
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.<br /> (© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Subjects :
- Adolescent
Adult
Cataract pathology
Child
Child, Preschool
Facies
Female
Growth Disorders pathology
Hearing Loss, Sensorineural pathology
Humans
Infant
Intellectual Disability pathology
Male
Musculoskeletal Abnormalities pathology
Mutation, Missense genetics
Young Adult
Cataract genetics
Genetic Predisposition to Disease
Growth Disorders genetics
Hearing Loss, Sensorineural genetics
Intellectual Disability genetics
Musculoskeletal Abnormalities genetics
Proto-Oncogene Proteins c-maf genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1399-0004
- Volume :
- 97
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Clinical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 31600839
- Full Text :
- https://doi.org/10.1111/cge.13651