- Login
- Register
- Home/Current Issue
- About the journal
- Editorial board
- Online submission
- Instructions for authors
- Subscriptions
- Foundation Acta Endocrinologica
- Archive
- Contact
Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
Acta Endocrinologica(Bucharest) is live in PubMed Central
Journal Impact Factor - click here.
This Article
Services
Google Scholar
PubMed
Acta Endocrinologica (Buc)
Almacan B, Ozdemir N, Onay H, Hekimsoy Z
Congenital Adrenal Hyperplasia with Compound Heterozygous I2 Splice and P453S Mutations
Acta Endo (Buc) 2022, 18 (2): 228-231doi: 10.4183/aeb.2022.228
Background. Congenital adrenal hyperplasia
(CAH) is an autosomal recessive inherited disorder caused
by congenital deficiency of enzymes involved in cortisol
biosynthesis from cholesterol in the adrenal cortex. In this
article, we aimed to present a 29-year-old female patient with
I2 splice point mutation detected in one allele and P453S
mutation on the other allele of CYP21A2 gene associated
with 21-hydroxylase deficiency. Her further investigation
revealed that her mother had P453S mutation and her father
had I2 splice mutation.
Case report. A 29-year-old woman with CAH was
admitted to our clinic with the request of pregnancy. Her
physical examination revealed a height of 151 cm, weight
59 kg, body mass index 25.8 kg/m2. According to Tanner
staging, she had Stage 3 breast development and pubic
hair. Her laboratory test results were as follows: Glucose:
79 mg/dL (70-100 mg/dL), Creatinine: 0.6 (0.5-0.95 mg/
dL), Sodium: 138 mEq/L (135-145 mEq/L), Potassium: 4.4
mEq/L (3.5-5.1 mEq/L), Cortisol: 0.05 μg/dL, ACTH: <5.00
pg/mL (5-46 pg/mL), 17-OH progesterone: 7.67 ng/mL (0-3
ng/mL). Chromosome analysis revealed a 46, XX karyotype.
CYP21A2 gene mutation analysis was performed for the
patient whose clinical history and laboratory results were
compatible with congenital adrenal hyperplasia. During the
reverse dot blot analysis, I2 splice mutation in one allele and
P453S mutation in the other allele were detected.
Conclusion. Although the I2 splice mutation
detected in our case was mostly associated with a saltwasting
form of CAH, it was thought that the other P453S
mutation detected may explain the relatively good clinical
course in our case.
Keywords: Congenital adrenal hyperplasia, P453S mutation, I2 splice mutation.
Correspondence: Burcu Almacan MD, Celal Bayar University, School of Medicine - Endocrinology, Manisa, 45040, Turkey, E-mail:
Burcu_almazcon@hotmail.com