ロード中...
Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations
Trichothiodystrophy (TTD) is a rare, autosomal recessive disease, characterised by brittle, sulfur deficient hair and multisystem abnormalities. A systematic literature review identified 112 patients ranging from 12 weeks to 47 years of age (median 6 years). In addition to hair abnormalities, common...
保存先:
| 主要な著者: | , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2008
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3459585/ https://ncbi.nlm.nih.gov/pubmed/18603627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2008.058743 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|