A Neonate Presenting with Severe Dehydration - A Case of Congenital Adrenal Hyperplasia with Salt Losing Crisis
Congenital adrenal hyperplasia (CAH) is a rare autosomal recessive disorder caused by mutations in genes involved in cortisol biosynthesis in the adrenal gland. Depending on the enzymatic defect, the symptoms, signs, and laboratory findings differ. The most common form, accounting for more than 95% of cases, is caused by 21-hydroxylase deficiency. Delay in the diagnosis and treatment can lead to life-threatening adrenal crisis with hemodynamic collapse. We report a case of a five-day-old male neonate with congenital adrenal hyperplasia and salt-wasting crisis. The diagnosis was made after comprehensive assessment of clinical features and laboratory investigations. He was treated with hydrocortisone and fludrocortisone and was discharged after one week.
Authors
- Manish Upreti (ORCID: https://orcid.org/0000-0002-1215-8150)
- Anita Lamichhane (ORCID: https://orcid.org/0000-0002-5279-9956)
- Rekha Phuyel
- Ramesh Khadka
Institutions
- Nepal Medical College Teaching Hospital (NP)
- Lumbini Medical College
Publication Details
- Journal
- Journal of Nepal Medical Association
- Published
- 2024-09-30
- DOI
- https://doi.org/10.31729/jnma.8777
- Primary Topic
- Sexual Differentiation and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00