Trichothiodystropohy-neurotrichocutaneous syndrome of Pollitt: A report of two unrelated cases

27Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

Two unrelated children presenting with mental and physical retardation and sulphur deficient brittle hair are reported. These are thought to be further cases of the autosomal recessive neurotrichocutaneous syndrome of Pollitt, of which eight cases have been previously reported.

Cite

CITATION STYLE

APA

King, M. D., Gummer, C. L., & Stephenson, J. B. P. (1984). Trichothiodystropohy-neurotrichocutaneous syndrome of Pollitt: A report of two unrelated cases. Journal of Medical Genetics, 21(4), 286–289. https://doi.org/10.1136/jmg.21.4.286

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free