✦ LIBER ✦

Alagille syndrome: case report with bilateral radio-ulnar synostosis and a literature review

✍ Scribed by R. S. Ryan; S. O. Myckatyn; G. D. Reid; P. Munk

Book ID: 105957960
Publisher: Springer
Year: 2003
Tongue: English
Weight: 139 KB
Volume: 32
Category: Article
ISSN: 0364-2348
DOI: 10.1007/s00256-003-0651-z

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Humero-radio-ulnar synostosis: A new cas

Humero-radio-ulnar synostosis: A new case and review

✍ Hersh, Joseph H. ;Joyce, Margie R. ;Profumo, Laura E. 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 259 KB 👁 1 views

Perinatal/Neonatal Case Presentation A N

Perinatal/Neonatal Case Presentation A Neonate with Severe Thrombocytopenia and Radio-Ulnar Synostosis

✍ Sola, Martha C; Slayton, William B; Rimsza, Lisa M; Perez, Jose A; Fuchs, Debora 📂 Article 📅 2005 🏛 Nature Publishing Group 🌐 English ⚖ 28 KB

Unilateral radio-ulnar synostosis, gener

Unilateral radio-ulnar synostosis, generalized hypotonia, and developmental delay with a characteristic facial appearance: A further case report

✍ Kannu, Peter ;Aftimos, Salim ;Der Kaloustian, Vazken M. 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 204 KB 👁 1 views

Crouzon syndrome: A case report and revi

Crouzon syndrome: A case report and review of literature

✍ Harroop Kaur; Harmeet Singh Waraich; Chander Mohan Sharma 📂 Article 📅 2006 🏛 Springer 🌐 English ⚖ 735 KB

Parsonage–Turner Syndrome—Case Report an

Parsonage–Turner Syndrome—Case Report and Literature Review

✍ A. J. Hussey; C. P. O’Brien; P. J. Regan 📂 Article 📅 2007 🏛 Springer-Verlag,Elsevier Science 🌐 English ⚖ 91 KB

A girl with metopic synostosis and triso

A girl with metopic synostosis and trisomy 13 mosaicism: Case report and review of the literature

✍ Ebru Aypar; M. Selman Yildirim; Ahmet Sert; Ilhan Ciftci; Dursun Odabas 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 175 KB 👁 1 views

## Abstract Trisomy 13, or Patau syndrome is a rare chromosomal disorder characterized by a triad of cleft lip and palate, postaxial polydactyly and microcephaly. Complete, partial, or mosaic forms of the disorder can occur. Mosaic trisomy 13 is very rare, it occurs in only 5% of all patients with