Neurofibromatosis presenting as painless clitoromegaly.
Copyright policy )Neurofibromatosis presenting as painless clitoromegaly.
Received June 2008 Accepted September 2008 INTRODUCTION Neurofibromatosis is an autosomal dominant progressive disorder with an incidence of approximately 1 in 3000 live births.(1) Its recognized features include hyperpigmented skin lesions (cafe-au-lait spots), neurofibromas, iris hamartomas, macrocephaly, central nervous system tumors, defects of the skull and facial bones, and vascular lesions. Involvement of the external genitalia is extremely unusual.(1,2) We present a case of a neurofibroma of the dorsal clitoral hood and its management.
- Children's Medical Center United States
- Children's Medical Center of Dallas United States
- The University of Texas Southwestern Medical Center United States
Neurofibromatosis 1, Child, Preschool, Humans, Female, RC870-923, Hypertrophy, Diseases of the genitourinary system. Urology, Clitoris
Neurofibromatosis 1, Child, Preschool, Humans, Female, RC870-923, Hypertrophy, Diseases of the genitourinary system. Urology, Clitoris
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