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Short stature in a 46,XX male adolescent / CJ Wu; YM Song; WH Sheu.-- p. 921-3.-- En: Southern Medical Journal.-- 92, 9 (1999)
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ADOLESCENTE   ESTATURA   INFORME DE CASO   TRASTORNOS DEL CRECIMIENTO   HORMONA DEL CRECIMIENTO   HUMANO   SINDROME DE KLINEFELTER   MASCULINO   LINAJE   ABERRACIONES DE CROMOSOMAS SEXUALES
Ubicación: Centro de Información y Documentación (CANIA)   
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    We describe a patient with a 46,XX karyotype who was assessed because of short stature and a subnormal rate of linear growth. The patient had normal male external genitalia. Endocrinologic analysis revealed elevated levels of luteinizing hormone and follicle-stimulating hormone but an exaggerated gonadotropin response to luteinizing hormone-releasing hormone stimulation. The growth hormone response to insulin-induced hypoglycemia was also exaggerated. All sequences examined on the sex-determining region Y gene were present. The diagnosis was 46,XX male with the major manifestation of short stature.

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