Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects.


Autoria(s): Wuyts W.; Waeber G.; Meinecke P.; Schüler H.; Goecke T.O.; Van Hul W.; Bartsch O.
Data(s)

2004

Resumo

The combination of multiple exostoses (EXT) and enlarged parietal foramina (foramina parietalia permagna, FPP) represent the main features of the proximal 11p deletion syndrome (P11pDS), a contiguous gene syndrome (MIM 601224) caused by an interstitial deletion on the short arm of chromosome 11. Here we present clinical aspects of two new P11pDS patients and the clinical follow-up of one patient reported in the original paper describing this syndrome. Recognised clinical signs include EXT, FPP, mental retardation, facial asymmetry, asymmetric calcification of coronary sutures, defective vision (severe myopia, nystagmus, strabismus), skeletal anomalies (small hands and feet, tapering fingers), heart defect, and anal stenosis. In addition fluorescence in situ hybridisation and molecular analysis were performed to gain further insight in potential candidate genes involved in P11pDS.

Identificador

http://serval.unil.ch/?id=serval:BIB_78E55FF453EC

isbn:1018-4813

pmid:14872200

doi:10.1038/sj.ejhg.5201163

isiid:000220879600012

Idioma(s)

en

Fonte

European Journal of Human Genetics, vol. 12, no. 5, pp. 400-406

Palavras-Chave #Abnormalities, Multiple; Adaptor Proteins, Signal Transducing; Adolescent; Adult; Child; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 11; Craniofacial Abnormalities; Exostoses, Multiple Hereditary; Female; Gene Deletion; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Male; Mental Retardation; N-Acetylglucosaminyltransferases; Nuclear Proteins; Parietal Bone; Syndrome; Trans-Activators
Tipo

info:eu-repo/semantics/article

article