Bleeding Diathesis in Hypotrichosis-Lymphedema-Telangiectasia Syndrome due to Decreased von Willebrand Factor.

Saved in:
Bibliographic Details
Title: Bleeding Diathesis in Hypotrichosis-Lymphedema-Telangiectasia Syndrome due to Decreased von Willebrand Factor.
Authors: Kanno M; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Sato H; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Uemura Y; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Meguro T; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Ishigaki R; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Kawasaki N; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Abiko M; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Suzuki K; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan., Numakura C; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan.; Department of Pediatrics and Clinical Genomics, Faculty of Medicine, Saitama Medical University, Saitama, Japan., Tamiya G; Department of AI and Innovative Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.; Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.; Statistical Genetics Team, RIKEN Center for Advanced Intelligence Project, Tokyo, Japan.; Department of Rare Disease Genomics, Tohoku University Graduate School of Medicine, Sendai, Japan., Takayama J; Department of AI and Innovative Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.; Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.; Statistical Genetics Team, RIKEN Center for Advanced Intelligence Project, Tokyo, Japan.; Department of Rare Disease Genomics, Tohoku University Graduate School of Medicine, Sendai, Japan., Kure S; Department of Rare Disease Genomics, Tohoku University Graduate School of Medicine, Sendai, Japan.; Miyagi Children's Hospital, Sendai, Japan., Saijo N; Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan., Kikuchi A; Department of Rare Disease Genomics, Tohoku University Graduate School of Medicine, Sendai, Japan.; Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan., Mitsui T; Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2026 Jun; Vol. 200 (6), pp. 1384-1387. Date of Electronic Publication: 2026 Jan 27.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1552-4833
DOI:10.1002/ajmga.70068