Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature-Reference-Cited by-同舟云学术

Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature

Published:2017-09-17 Issue:9 Volume:18 Page:1998
ISSN:1422-0067
Container-title:International Journal of Molecular Sciences
language:en
Short-container-title:IJMS

Author:

Prontera Paolo,Rogaia Daniela,Mencarelli Amedea,Ottaviani Valentina,Sallicandro Ester,Guercini Giorgio,Esposito Susanna,Bersano Anna,Merla Giuseppe,Stangoni Gabriela

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Link

http://www.mdpi.com/1422-0067/18/9/1998/pdf

Reference34 articles.

1. Cerebrovascular "Moyamoya" Disease

2. Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians

3. Prevalence and Characteristics of Concurrent Down Syndrome in Patients With Moyamoya Disease

4. Moyamoya syndrome in a Caucasian woman with Turner's syndrome

5. Complex Chromosome Rearrangement of 6p25.3->p23 and 12q24.32->qter in a Child With Moyamoya

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