MIDAS Syndrome (Microphthalmia with Linear Skin Defects)
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-87893-1_18
Reference14 articles.
1. Al-Gazali LI, Muller RF, Caine A, et al. An XX male and two t (X;Y) females with linear skin defects and congenital microphthalmia in a new syndrome at Xp22.3. Med Genet. 1988;25:638–42.
2. van Rahden VA, Fernandez-Vizarra E, Alawi M. Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome. Am J Hum Genet. 2015;96:640–50.
3. Banganho D, Oliveira I, Machado C, Póvoas M. Microphthalmia with linear skin defects (MLS) syndrome: familial presentation. BMJ Case Rep. 2019;12:e227791.
4. Durack A, Mehta SG, Allen LE, et al. Linear skin defects and microphthalmia. Clin Exp Dermatol. 2018;43:860–2.
5. Kumar P, Rajab A. Microphthalmia with linear skin defects (MLS) syndrome: familial presentation. Clin Exp Dermatol. 2018;43:196–7.
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