Brittle hair, developmental delay, neurologic abnormalities, and photosensitivity in a 4-year-old girl - 24/04/13
Doi : 10.1016/j.jaad.2010.03.041
Xiaolong Zhou, MSc a, b, Sikandar G. Khan, PhD a, Deborah Tamura, RN, MS a, Nicholas J. Patronas, MD c, Wadih M. Zein, MD d, Brian P. Brooks, MD, PhD d, Kenneth H. Kraemer, MD a, ⁎ 
, John J. DiGiovanna, MD a, e
, John J. DiGiovanna, MD a, e a DNA Repair Section, Dermatology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
b Clinical Research Training Program, National Institutes of Health, Bethesda, Maryland
c Department of Radiology, Clinical Center, National Institutes of Health, Bethesda, Maryland
d National Eye Institute, National Institutes of Health, Bethesda, Maryland
e Division of Dermatopharmacology, Department of Dermatology, The Warren Alpert School of Medicine of Brown University, Providence, Rhode Island
Reprint requests: Kenneth H. Kraemer, MD, Dermatology Branch, National Cancer Institute, Bldg 37, Room 4002, Bethesda, MD 20892.Key words : collodion membrane, congenital ichthyosis, DNA repair, erythroderma, genetic diseases, hair abnormalities, recurrent infections, trichothiodystrophy
Abbreviations used : MRI, NIH, TTD, XP
Plan
| Supported by the Intramural Research Programs of the Center for Cancer Research, National Cancer Institute, National Institutes of Health (NIH). Support for Mr Zhou was made possible through the Clinical Research Training Program, a public-private partnership supported jointly by the NIH and Pfizer Inc (via a grant to the Foundation for NIH from Pfizer Inc). |
|
| Conflicts of interest: None declared. |
© 2010
American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 63 - N° 2
P. 323-328 - août 2010 Retour au numéro
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