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
收藏
页码：25 / 27
页数：3
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