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Vol. 101. Núm. 7.
Páginas 637-640 (septiembre 2010)
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Vol. 101. Núm. 7.
Páginas 637-640 (septiembre 2010)
Case report
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New Mutation in the Birt Hogg Dube Gene
Nueva mutación en el síndrome de Birt Hogg Dubé
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L. Sempaua,
Autor para correspondencia
leticiasempau@gmail.com

Corresponding author.
, I. Ruiza, A. González-Moránb, X. Susannac, T.V.O. Hansend
a Servicio de Dermatología, Complejo Asistencial de León, León, Spain
b Servicio de Anatomía Patológica, Complejo Asistencial de León, León, Spain
c Director Técnico de Balagué Center, Barcelona, Spain
d Department of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark
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Abstract

Patients with Birt-Hogg-Dube syndrome have an increased risk of developing hamartomas of the pilosebaceous unit, renal tumors of various types, lung cysts, and spontaneous pneumothorax. We present the case of a 54-year-old woman with a long history of whitish papules in the central region of the face and a family history of similar lesions. Biopsy and genetic study revealed a new mutation of the gene involved in Birt-Hogg-Dube syndrome.

Keywords:
Fibrofolliculoma
Acrochordon
Birt-Hogg-Dube syndrome
Mutation
Resumen

El Birt Hogg Dubé es un síndrome que predispone a la aparición de hamartomas del folículo pilosebáceo y a mayor riesgo de presentar tumores renales de diversa estirpe, quistes pulmonares y neumotórax espontáneos.

Presentamos el caso de una mujer de 54 años que presenta desde hace años pápulas blanquecinas centrofaciales e historia familiar de esas mismas pápulas. Tras biopsia y estudio genético de la paciente se detecta una nueva mutación en el gen implicado en este síndrome.

Palabras clave:
Fibrofoliculoma
Acrocordón
Síndrome Birt Hogg Dubé
Mutación
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Copyright © 2010. Academia Española de Dermatología y Venereología and Elsevier España, S.L.
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