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Clinical Consequences in Truncating Mutations in Exon 34 of NOTCH2: Report of Six Patients With Hajdu-Cheney Syndrome and a Patient With Serpentine Fibula Polycystic Kidney Syndrome

Authors
 Yoko Narumi ; Byung-Joo Min ; Gen Nishimura ; Woong-Yang Park ; Yoshimitsu Fukushima ; Ok-Hwa Kim ; Yoon-Sok Chung ; Yumie Rhee ; Tomoki Kosho ; Koichi Nakamura ; Kiyoko Sameshima ; Itsuro Kazukawa ; Kenji Shimizu 
Citation
 American Journal of Medical Genetics part A, Vol.161A(3) : 518~526, 2013 
Journal Title
 American Journal of Medical Genetics part A 
ISSN
 1552-4825 
Issue Date
2013
Abstract
It is debatable whether Hajdu-Cheney syndrome (HCS) and serpentine fibula-polycystic kidney syndrome (SFPKS) represent a single clinical entity with a variable degree of expression or two different entities, because both disorders share common clinical and radiological manifestations, including similar craniofacial characteristics, and defective bone mineralization. Since it was shown that heterozygous truncating mutations in NOTCH2 are responsible for both HCS and SFPKS, 37 patients with HCS and four patients with SFPKS are reported. To elucidate the clinical consequences of NOTCH2 mutations, we present detailed clinical information for seven patients with truncating mutations in exon 34 of NOTCH2, six with HCS and one with SFPKS. In addition, we review all the reported patients whose clinical manifestations are available. We found 13 manifestations including craniofacial features, acroosteolysis, Wormian bones, and osteoporosis in >75% of NOTCH2-positive patients. Acroosteolysis was observed in two patients with SFPKS and bowing fibulae were found in two patients with HCS. These clinical and molecular data would support the notion that HCS and SFPKS are a single disorder
URI
http://ir.ymlib.yonsei.ac.kr/handle/22282913/87881
DOI
10.1002/ajmg.a.35772
Appears in Collections:
1. 연구논문 > 1. College of Medicine > Dept. of Internal Medicine
Yonsei Authors
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Link
 http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35772/abstract
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