Stüve-Wiedemann syndrome in a neonate
Author:
Affiliation:
1. 1st Department of Neonatology; Aristotle University of Thessaloniki; Thessaloniki Greece
2. Center for Human Genetics; Freiburg Germany
3. 1st Department of Pediatrics; Aristotle University of Thessaloniki; Thessaloniki Greece
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12431/fullpdf
Reference17 articles.
1. Null leukemia inhibitory factor receptor (LIFR) mutations in Stuve-Wiedemann/Schwartz-Jampel type 2 syndrome;Dagoneau;Am. J. Hum. Genet.,2004
2. Neonatal Schwartz-Jampel syndrome: A common autosomal recessive syndrome in the United Arab Emirates;Al-Gazali;J. Med. Genet.,1996
3. Presentation of six cases of Stüve-Wiedemann syndrome;Cormier-Daire;Pediatr. Radiol.,1998
4. Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: A case for “lumping”;Superti-Furga;Am. J. Med. Genet.,1998
5. Stüve-Wiedemann syndrome in children surviving infancy: Clinical and radiological features;Al-Gazali;Clin. Dysmorphol.,2003
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Paediatric survivors beyond infancy with Stüve-Wiedemann syndrome – A case series from the West Midlands, UK;European Journal of Medical Genetics;2023-08
2. Clinical overview and outcome of the Stuve-Wiedemann syndrome: a systematic review;Orphanet Journal of Rare Diseases;2022-04-23
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