Trichothiodystrophy
Author:
Publisher
Springer London
Link
http://link.springer.com/content/pdf/10.1007/978-1-4471-4486-1_14.pdf
Reference12 articles.
1. Itin PH, Sarasin A, Pittelkow MR. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes. J Am Acad Dermatol. 2001;44(6):891–920; quiz 1–4.
2. Price VH, Odom RB, Ward WH, Jones FT. Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex. Arch Dermatol. 1980;116(12):1375–84.
3. Morice-Picard F, Cario-Andre M, Rezvani H, Lacombe D, Sarasin A, Taieb A. New clinico-genetic classification of trichothiodystrophy. Am J Med Genet A. 2009;149A(9):2020–30.
4. Zhou X, Khan SG, Tamura D, Patronas NJ, Zein WM, Brooks BP, et al. Brittle hair, developmental delay, neurologic abnormalities, and photosensitivity in a 4-year-old girl. J Am Acad Dermatol. 2010;63(2):323–8.
5. Itin PH, Fistarol SK. Hair shaft abnormalities—clues to diagnosis and treatment. Dermatology. 2005;211(1):63–71.
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