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Trichothiodystrophy with sideroblastic anaemia and developmental delay.

A patient with sideroblastic anaemia, development delay, and trichothiodystrophy is presented. Trichothiodystrophy is a feature of several autosomal recessive diseases. Photosensitivity, failure to thrive, and developmental delay are commonly observed in affected cases. X linked inheritance accounts...

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Bibliografski detalji
Glavni autori: Lynch, S A, de Berker, D, Lehmann, A R, Pollitt, R J, Reid, M M, Lamb, W H
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1511270/
https://ncbi.nlm.nih.gov/pubmed/7492166
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