1.Management of Congenital Adrenal Hyperplasia.
Journal of Korean Society of Pediatric Endocrinology 2003;8(1):15-26
No abstract available.
Adrenal Hyperplasia, Congenital*
2.Congenital Adrenal Hyperplasia in Korea.
Journal of Korean Society of Pediatric Endocrinology 2005;10(2):132-137
No abstract available.
Adrenal Hyperplasia, Congenital*
;
Korea*
3.Two Cases of the Salts Losing Congenital Adrenal Hyperplasia.
Journal of the Korean Pediatric Society 1981;24(11):1092-1099
No abstract available.
Adrenal Hyperplasia, Congenital*
;
Salts*
4.Adrenaogenital Syndrome with Congenital Adrenal Hyperplasia.
Kyeong Rae MOON ; Yeong Bong PARK ; Sang Gi KIM ; Jin Heon KIM ; Chang Soo RA ; Jae Hong SEO ; Ho Won HWANG
Journal of the Korean Pediatric Society 1985;28(1):78-84
No abstract available.
Adrenal Hyperplasia, Congenital*
5.Congenital adrenal Hyperplasia.
Byoung Hai AHN ; Sei Won YANG ; Hyung Ro MOON
Journal of the Korean Pediatric Society 1986;29(6):22-30
No abstract available.
Adrenal Hyperplasia, Congenital*
6.Two Cases of The Salt-losing Congenital Adrenal Hyperplasia.
Sung Hun EUN ; Cheong Min LEE ; Young Chang TOCKGO ; Hyun Keum LEE
Journal of the Korean Pediatric Society 1985;28(5):499-504
No abstract available.
Adrenal Hyperplasia, Congenital*
7.Clinical Presentation of Congenital Adrenal Hyperplasia in Selected Multiethnic Paediatric Population
Subashini Chellappah Thambiah ; Zalinah Ahmad ; Zarida Hambali ; Malina Osman ; Munira Mohd Zain ; Fuziah Md Zain ; Janet Hong Yeow Hua
Malaysian Journal of Medicine and Health Sciences 2015;11(1):77-83
A clinical descriptive study was done to determine the sociodemographic, laboratory and clinical
characteristics of patients with congenital adrenal hyperplasia (CAH) referred to Hospital Putrajaya, a
tertiary endocrine centre in Malaysia. Electronic laboratory data of 51 CAH patients were obtained. The
demographics and clinical details of the study population were acquired from a questionnaire completed
by parents of participants. There were 25 males (49%) and 26 females (51%), of which, 58.8% were
Malays. Median age of participants was 4 years whilst median age at diagnosis of CAH was two years.
Parental consanguinity was documented in three patients (5.9%). Patients originated from Johor (19.6%),
Selangor (19.6%), Negeri Sembilan (17.6%) and Kedah (13.7%). Majority of patients were diagnosed
after one week of life (80.4%) although more females were diagnosed under the age of one week
compared to males (p=0.041). Most females presented with ambiguous genitalia (42.3%) [p=0.001]
whereas 72% of males presented with salt wasting (p=0.003). No significant associations between race
and all other variables, though interestingly three Malay patients presented with ambiguous genitalia
and hypertension. Equal gender distribution noted as expected in an autosomal recessive condition,
although not in keeping with other Asian countries. Early diagnosis in females attributed to obvious
genital ambiguity at birth. Varied clinical presentation, although in minority, necessitates genetic studies
for prompt diagnosis and treatment. Considering that majority of patients presented with salt wasting
and the age at diagnosis was delayed, the introduction of a neonatal screening programme is essential
in Malaysia.
Adrenal Hyperplasia, Congenital
8.Adrenogenital Syndrome with Congenital Adrenal Hyperplasia.
Myoung Sung MOON ; Kwang Nam KIM ; Woo Gill LEE
Journal of the Korean Pediatric Society 1984;27(5):511-515
No abstract available.
Adrenal Hyperplasia, Congenital*
;
Adrenogenital Syndrome*
9.Diagnosis by serendipity: A case of mosaic turner syndrome and late onset congenital adrenal hyperplasia
Kimberly C. Lu Chiu, RPm, MD ; Susana S. Lao, MD, FPOGS, FPSREI, FPSGE ; Irene Y. Sy, MD, FPOGS, FPSREI, FPSGE
Philippine Journal of Reproductive Endocrinology and Infertility 2023;20(1):29-37
Congenital Adrenal Hyperplasia and Turner Syndrome are not very rare diseases. However, their
combination may be confounding. Presented here is a case of a 54 year old nulligravid, with
primary amenorrhea, short stature, absent breast development, hirsutism, signs of virilization,
and clitoromegaly who came in due to hypogastric pain and an enlarging palpable hypogastric
mass. Diagnostic procedures and surgical management are discussed.
Congenital Adrenal Hyperplasia
;
Turner Syndrome