Sexual ambiguity by salt-wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A case report

被引：0

作者：

Abarca-Acuna, Bryan ^{[1
]}

Delgado-Valencia, Edison ^{[1
]}

Atamari-Anahui, Noe ^{[1
]}

Zea-Nunez, Carlos ^{[1
,2
]}

机构：

[1] Univ Nacl San Antonio Abad del Cusco, Fac Med Humana, Cuzco, Peru

[2] Hosp Adolfo Guevara Velasco, Essalud Cusco, Peru

来源：

REVISTA DEL CUERPO MEDICO DEL HOSPITAL NACIONAL ALMANZOR AGUINAGA ASENJO | 2015年 / 8卷 / 01期

关键词：

Disorders of Sex Development; Congenital Adrenal Hyperplasia; Steroid 21-Hydroxylase (Source: MeSH-NLM);

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Introduction: Disorders of sexual differentiation by congenital adrenal hyperplasia are relatively common and require proper care to ensure both rapid diagnosis and management of possible disorders that accompany them. Report: 18 days old patient comes with excessive weight loss, dehydration, ambiguous genitalia. Interpretation: Salt-wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency was diagnosed, a very rare case in our environment and it is important to identify it as soon as possible.

引用

页码：25 / 27

页数：3

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