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Titel:

Anal atresia, coloboma, microphthalmia, and nasal skin tag in a female patient with 3.5 Mb deletion of 3q26 encompassing SOX2.

Dokumenttyp:
Journal Article
Autor(en):
Salem, Nabeel J M; Hempel, Maja; Heiliger, Katrin-Janine; Hosie, Stuart; Meitinger, Thomas; Oexle, Konrad
Abstract:
A full term female newborn presented with prominent forehead, bilateral microphthalmia, iris coloboma and cataract, wide intercanthal distance, large, low-set and protruding ears, skin tag at the left nasal nostril, imperforate anus with rectovestibular fistula, and postnatal growth delay with brachymicrocephaly. A marker chromosome was not detectable and the copy number of 22q11 was normal. However, array CGH revealed a 3.5 Mb microdeletion of chromosome region 3q26.32-3q26.33 (chr. 3: 178,598,...     »
Zeitschriftentitel:
Am J Med Genet A
Jahr:
2013
Band / Volume:
161A
Heft / Issue:
6
Seitenangaben Beitrag:
1421-4
Sprache:
eng
Volltext / DOI:
doi:10.1002/ajmg.a.35883
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/23613260
Print-ISSN:
1552-4825
TUM Einrichtung:
Institut für Humangenetik
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