Rare and Atypical Findings in Smith-Magenis Syndrome: A Case Report

Author:

KALAYCI YİĞİN Aysel,ALAY Tarık,SEVEN Mehmet

Publisher

Journal of Medical, published by Ibrahim Ikizceli

Subject

General Medicine

Reference13 articles.

1. 1. Elsea SH, Girirajan S. Smith–Magenis syndrome. European Journal of Human Genetics. 2008; 16(4), 412–421.

2. 2. Falco M, Amabile S, Acquaviva F. RAI1 gene mutations: mechanisms of Smith-Magenis syndrome. Appl Clin Genet. 2017; 10:85-94.

3. 3. Greenberg F, Guzzetta V, Montes de Oca-Luna R, Magenis RE, Smith AC, Richter SF et al. Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2). Am J Hum Genet. 1991; 49(6):1207-18.

4. 4. Chen L, Mullegama SV, Alaimo JT, Elsea SH. Smith-Magenis syndrome and its circadian influence on development, behavior, and obesity - own experience. Dev Period Med. 2015; 19(2):149-56. Review.

5. 5. Smith AC, Dykens E, Greenberg F. Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2). Am J Med Genet. 1998; 81(2):186- 191.

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