Literature DB >> 16141486

Acrodysostosis: autosomal dominant transmission.

S R Sheela1, Ajai Perti, Grace Thomas.   

Abstract

We describe a two and half year old male child with acrodysostosis, presenting with nasal hypoplasia, peripheral dysostosis (gross shortening of hands and feet), cone-shaped epiphysis, advanced bone age, and mental retardation. He and his mother also had bilateral first ray hyperplasia of the feet thereby expressing the autosomal dominant inheritance pattern.

Entities:  

Mesh:

Year:  2005        PMID: 16141486

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  3 in total

1.  Exome sequencing identifies PDE4D mutations in acrodysostosis.

Authors:  Hane Lee; John M Graham; David L Rimoin; Ralph S Lachman; Pavel Krejci; Stuart W Tompson; Stanley F Nelson; Deborah Krakow; Daniel H Cohn
Journal:  Am J Hum Genet       Date:  2012-03-29       Impact factor: 11.025

2.  Expanding the phenotypic spectrum of variants in PDE4D/PRKAR1A: from acrodysostosis to acroscyphodysplasia.

Authors:  Caroline Michot; Carine Le Goff; Edward Blair; Patricia Blanchet; Yline Capri; Brigitte Gilbert-Dussardier; Alice Goldenberg; Alex Henderson; Bertrand Isidor; Hulya Kayserili; Esther Kinning; Martine Le Merrer; Stanislas Lyonnet; Sylvie Odent; Pelin Ozlem Simsek-Kiper; Chloé Quelin; Ravi Savarirayan; Marleen Simon; Miranda Splitt; Judith M A Verhagen; Alain Verloes; Arnold Munnich; Geneviève Baujat; Valérie Cormier-Daire
Journal:  Eur J Hum Genet       Date:  2018-07-13       Impact factor: 4.246

3.  The first mutation identified in a Chinese acrodysostosis patient confirms a p.G289E variation of PRKAR1A causes acrodysostosis.

Authors:  Nan Li; Min Nie; Mei Li; Yan Jiang; Xiaoping Xing; Ou Wang; Chunlin Li; Weibo Xia
Journal:  Int J Mol Sci       Date:  2014-07-29       Impact factor: 5.923

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.