Abstract |
The androgen resistance syndrome, is a dominant and recessive linked to X disorder, with clinically heterogenous manifestations. Reported case. A 17-years patient with primary amenorrhoea and genital ambiguity. Bilateral inguinal herniplastia and probable gonadectomy were performed at 14-months-old. His cariotipe was male 46,XY and the hormonal determinations showed the presence of hypergonadotropic hypogonadismo. The congenital adrenal hyperplasia (deficiency of 21-hidroxilase) was discarded. In the partial androgen resistance syndrome, the prepuberal gonadectomy avoid a progresive virilization of the external genitals. However, the estrogenic hormonal replacement is mandatory.
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Authors | M A Garcia Morales, J Barron Vallejo, L Limon Luque |
Journal | Ginecologia y obstetricia de Mexico
(Ginecol Obstet Mex)
Vol. 64
Pg. 120-1
(Mar 1996)
ISSN: 0300-9041 [Print] Mexico |
Vernacular Title | Efecto de la gonadectomía prepuberal en el Síndrome de Resistencia Parcial a los Andrógenos. |
PMID | 8729188
(Publication Type: Case Reports, English Abstract, Journal Article)
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Chemical References |
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Topics |
- Adolescent
- Age Factors
- Disorders of Sex Development
(metabolism, physiopathology)
- Estrogen Replacement Therapy
- Female
- Gonads
(surgery)
- Humans
- Hypogonadism
(etiology)
- Infant
- Karyotyping
- Male
- Receptors, Androgen
- Syndrome
- X Chromosome
- Y Chromosome
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