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          Document History for Document ID 539471

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Document Version Version Comment Date Status
539471.0 [No comment] 09.03.2011 11:53 Released

ID: 539471.0, MPI für molekulare Genetik / Research Group Development and Disease
A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.
Authors:Kantaputra, P. N.; Mundlos, S.; Sripathomsawat, W.
Language:English
Date of Publication (YYYY-MM-DD):2010-10-14
Title of Journal:American Journal of Medical Genetics Part A
Journal Abbrev.:Am J Med Genet A
Volume:152A
Issue / Number:11
Start Page:2832
End Page:2837
Copyright:© 2010 Wiley-Liss, Inc.
Review Status:not specified
Audience:Experts Only
Abstract / Description:Al-Awadi/Raas-Rothschild/Schinzel phocomelia (AARRS) syndrome, a rare autosomal recessive disorder, comprises malformations of upper and lower limbs with severely hypoplastic pelvis and abnormal genitalia. Mutations in WNT7A have been reported as cause of the syndrome. We report on two sisters in a Thai family with short and malformed long bones, absent fibulae, flexion contracture of digits, and a/hypoplastic nails. Fusion between severely malformed femora and slender tibiae has never been reported in patients with WNT7A mutations. Lower limbs were more severely malformed than the upper ones and the pelvis was also severely affected. Multiple fusions of long bones and of the femoral heads to the acetabula were evident. A novel homozygous missense mutation in coding exon 4 of the WNT7A was detected in both affected daughters (c.664C > T) leading to an amino acid exchange from arginine to tryptophan (p.Arg222Trp; R222W). The phenotype is likely to result from an abnormality of all three signaling centers in the developing limb resulting in ventralization with a loss of dorsal structures (aplasia/hypoplasia of nails) a loss of anterior-posterior identity (single distal bones in lower limb without polarity) and an outgrowth defect resulting in distal truncations.
Free Keywords:absent fibula;
absent tarsal bones;
fusion of bones;
hypoplastic nails;
limb anomaly;
malformed pelvis
Comment of the Author/Creator:Correspondence: Piranit N. Kantaputra, Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry; Craniofacial Genetics Laboratory, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand.
External Publication Status:published
Document Type:Article
Communicated by:Stefan Mundlos
Affiliations:MPI für molekulare Genetik
External Affiliations:1.Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry; Craniofacial Genetics Laboratory, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand;
2.Institut für Medizinische Genetik, Charité Universitätsmedizin Berlin, Berlin, Germany.
Identifiers:ISSN:1552-4825 [ID No:1]
URL:http://www.ncbi.nlm.nih.gov/pubmed/20949531 [ID No:2]
DOI:10.1002/ajmg.a.33673 [ID No:3]
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