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Deletion mapping of split hand/split foot malformation with hearing impairment: a case report.

Authors :
Fukushima K
Nagai K
Tsukada H
Sugata A
Sugata K
Kasai N
Kibayashi N
Maeda Y
Gunduz M
Nishizaki K
Source :
International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2003 Oct; Vol. 67 (10), pp. 1127-32.
Publication Year :
2003

Abstract

Split hand/split foot malformation (SHFM), which typically appears as lobster-like limb malformation, is a rare clinical condition caused by a partial deletion of chromosome 7q. Hearing impairment sometimes accompanies syndromic SHFM cases; a case of inner and middle ear malformation with SHFM is described in this report. We conducted a genetic evaluation of this patient and found a deleted region that overlaps a previously reported locus of SHFM as well as a DFNB14 locus that can cause nonsyndromic hearing impairment by autosomal recessive inheritance.

Details

Language :
English
ISSN :
0165-5876
Volume :
67
Issue :
10
Database :
MEDLINE
Journal :
International journal of pediatric otorhinolaryngology
Publication Type :
Academic Journal
Accession number :
14550969
Full Text :
https://doi.org/10.1016/s0165-5876(03)00193-9