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Cutis ; 97(2): E10-3, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26919505

RESUMEN

Bloom syndrome, a rare autosomal-recessive disorder, characteristically presents with photosensitivity, telangiectatic facial erythema, and growth deficiency. We present a case of Bloom syndrome with uncommon clinical manifestations including alopecia areata, eyebrow hair loss, flat nose, reticular pigmentation, and short sharpened distal phalanges with fingernails that were wider than they were long. We detected the Bloom syndrome gene, BLM, which is one of the members of the RecQ family of DNA helicases, and found changes in 2 heterozygous nucleotide sites in the patient as well as her father and mother.


Asunto(s)
Síndrome de Bloom/diagnóstico , Dermatosis Facial/etiología , Pruebas Genéticas/métodos , Vesícula/etiología , Vesícula/patología , Síndrome de Bloom/genética , Síndrome de Bloom/patología , Niño , Eritema/etiología , Eritema/patología , Dermatosis Facial/patología , Femenino , Humanos
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