4.5 Article

Skeletal abnormalities are common features in Ayme-Gripp syndrome

Journal

CLINICAL GENETICS
Volume 97, Issue 2, Pages 362-369

Publisher

WILEY
DOI: 10.1111/cge.13651

Keywords

Ayme-Gripp syndrome; bone defects; MAF; skeletal dysplasia

Funding

  1. Fondazione Bambino Gesu, Vite coraggiose
  2. Italian Ministry of Health, Ricerca Corrente 2019

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Ayme-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.

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