Khan Sarah, Tafweez Raafea, Haider Areiba, Yaqoob Muhammad
Dr. Sarah Khan, MBBS, M-Phil Anatomy Assistant Professor of Anatomy, Department of Anatomy, King Edward Medical University, Lahore, Pakistan.
Dr. Raafea Tafweez, MBBS, M-Phil, FCPS, PhD. Professor of Anatomy, Department of Anatomy, King Edward Medical University, Lahore, Pakistan.
Pak J Med Sci. 2021 Jan-Feb;37(1):244-249. doi: 10.12669/pjms.37.1.2991.
To describe the mode of presentation and frequency of external genital anomalies in disorder of sex development (DSD).
This cross-sectional study was conducted at Children Hospital & Institute of Child Health, Lahore from January to December, 2016 on Children with DSD above 10 years of age. A detailed history and physical examination were done. Positive findings were recorded on a predesigned proforma and analyzed by SPSS 21. Karyotyping on blood samples was done to determine their genetic sex.
Out of 83 DSD children, 67% (n=56) were assigned a female sex at birth of which 9% (n=5) had ambiguous genitalia. Male sex at birth was given to 33% (n=27) of which 96% (n=26) had genital ambiguity. Mode of presentation other than ambiguous genitalia were delayed puberty, amenorrhea, hirsuitism, gynaecomastia, cyclic hematuria etc. Clitoromegaly was the main finding in 62.5% (n=5) and micropenis in 45% (n=9). Karyotypic sex of 56 female sex of rearing was 46XX 80% (n=45), 45X0 13% (n=7), XXX 2% (n=1) and 46 XY in 5% (n=3). Karyotypic sex of 27 male sex of rearing was 46XY in 78% (n=21), 46XX in 15% (n=4) and 47XXY in 7% (n=2).
Disorders of sex development presented with a wide spectrum of external genital anomalies ranging from clitoromegaly in females to micropenis and hypospadias in males. There was also an extreme diversity in mode of presentation of these cases including pubertal delay, amenorrhea in females and gender confusion disorders.
描述性发育障碍(DSD)中外生殖器异常的表现形式及发生率。
本横断面研究于2016年1月至12月在拉合尔儿童医院及儿童健康研究所对10岁以上的DSD患儿进行。进行了详细的病史采集和体格检查。阳性结果记录在预先设计的表格上,并采用SPSS 21进行分析。采集血样进行核型分析以确定其遗传性别。
在83例DSD患儿中,67%(n = 56)出生时被指定为女性,其中9%(n = 5)有生殖器模糊。33%(n = 27)出生时被指定为男性,其中96%(n = 26)有生殖器模糊。除生殖器模糊外的表现形式有青春期延迟、闭经、多毛症、男性乳房发育、周期性血尿等。阴蒂肥大是62.5%(n = 5)的主要表现,小阴茎是45%(n = 9)的主要表现。56例抚养性别为女性的患儿核型性别为46XX的占80%(n = 45),45X0的占13%(n = 7),XXX的占2%(n = 1),46 XY的占5%(n = 3)。27例抚养性别为男性的患儿核型性别为46XY的占78%(n = 21),46XX的占15%(n = 4),47XXY的占7%(n = 2)。
性发育障碍表现为广泛的外生殖器异常,从女性的阴蒂肥大到男性的小阴茎和尿道下裂。这些病例的表现形式也极具多样性,包括青春期延迟、女性闭经和性别混淆障碍。