Infantile systemic hyalinosis in identical twins-Reference-Cited by-同舟云学术

Infantile systemic hyalinosis in identical twins

Published:2015 Issue:4 Volume:4 Page:210-213
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Koonuru Mahesh Kumar¹,Venugopal Satya Prasad²

Affiliation:

1. SV Physiotherapy and Early intervention center for Children with Special Needs

2. MNR Medical College and Hospital

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/4/4/4_2015.01027/_pdf

Reference19 articles.

1. 1. Büyükgebiz B, Oztürk Y, Arslan N, Ozer E. A rare cause of protein-losing enteropathy and growth retardation in infancy: Infantile systemic hyalinosis. Turk J Pediatr. 2003; 45:258-260.

2. 2. Hanks S, Adams S, Douglas J, et al. Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Am J Hum Genet. 2003; 73:791-800.

3. 3. Rahman N, Dunstan M, Teare MD, et al. The gene for juvenile hyaline fibromatosis maps to chromosome 4q21. Am J Hum Genet. 2002; 71:975-980.

4. 4. Huang YC, Xiao YY, Zheng YH, Jang W, Yang YL, Zhu XJ. Infantile systemic hyalinosis: A case report and mutation analysis in a Chinese infant. Br J Dermatol. 2007; 156:602-604.

5. 5. Al-Mayouf SM, AlMehaidib A, Bahabri S, Shabib S, Sakati N, Teebi AS. Infantile systemic hyalinosis: A fatal disorder commonly diagnosed among Arabs. Clin Exp Rheumatol. 2005; 23:717-720.

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