Title: Tetra-amelia and lung hypo/aplasia syndrome: New case report and review
Authors: Sousa, Sérgio B. 
Pina, Raquel 
Ramos, Lina 
Pereira, Naigel 
Krahn, Martin 
Borozdin, Wiktor 
Kohlhase, Jürgen 
Amorim, Marta 
Gonnet, Katia 
Lévy, Nicolas 
Carreira, Isabel M. 
Couceiro, Ana Bela 
Saraiva, Jorge M. 
Issue Date: 2008
Citation: American Journal of Medical Genetics Part A. 9999:9999 (2008) n/a
Abstract: Tetra-amelia is a rare malformation that may be associated with other anomalies and is usually inherited in an autosomal recessive pattern. We describe a fetus, born to a nonconsanguineous couple, with tetra-amelia, bilateral cleft lip and palate and bilateral lung agenesis, without other anomalies. Karyotype was normal (46,XX) and premature centromere separation was excluded. No mutation was identified upon molecular analysis of WNT3, HS6ST1, and HS6ST3. We reviewed the literature and the differential diagnosis to clarify the clinical delineation of conditions associated with tetra-amelia. The present report describes the sixth family with this pattern of malformations and reinforces the evidence that the ldquotetra-amelia and lung hypo/aplasia syndromerdquo is a distinct autosomal recessive condition, with no identified gene thus far. © 2008 Wiley-Liss, Inc.
URI: http://hdl.handle.net/10316/8440
Rights: openAccess
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais

Files in This Item:
File Description SizeFormat 
obra.pdf134.3 kBAdobe PDFView/Open
Show full item record
Google ScholarTM
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.