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Transient salt wasting in POMC-deficiency due to infection induced stress
Insights
Pro-opiomelanocortin (POMC) deficiency causes severe obesity and hypoglycemia in infants. Early hydrocortisone treatment resolves these issues but requires monitoring for mineralocorticoid deficiency during stress.
Area of Science:
- Endocrinology
- Genetics
- Pediatrics
Background:
- Obesity is a complex condition with diverse etiologies.
- Pro-opiomelanocortin (POMC) deficiency is a rare genetic disorder leading to early-onset obesity and hormonal imbalances.
Observation:
- A 12-month-old male presented with severe obesity, hyperphagia, irritability, and a history of neonatal hypoglycemia.
- Clinical features included red hair, overgrowth syndrome, and hypocortisolism.
- Delayed motor skills were attributed to obesity.
Findings:
- The patient was diagnosed with POMC deficiency, confirmed by genetic testing.
- Hydrocortisone therapy resolved hypoglycemia and apnea episodes.
- Relative mineralocorticoid deficiency occurred during a urinary tract infection.
Implications:
- Early diagnosis and treatment of POMC deficiency are crucial for managing severe obesity and related complications.
- Monitoring for and managing relative mineralocorticoid deficiency during stress is essential in patients with POMC deficiency.
- Genetic counseling and long-term follow-up are recommended for affected individuals and families.
Abstract:
Obesity is a multifactorial disorder influenced by genetic, behavioral, environmental and cultural factors. A twelve month old male patient was admitted to the hospital because of malaise, irritability, disquietness and obesity. His BMI was 19.8 kg/m (2) and BMI SDS was 1.38. Mental development was normal, and motor skills were mildly delayed most probably due to his obesity. His physical examination was totally normal except obesity and red hair. A history of hypoglycemia on the fourth day of life, which resolved after oral glucose administration, was reported. The child had been hyperphagic from the first weeks of life and had aggressive behavior when food was denied. The body weight of the patient increased dramatically during the first year of life. Based on the clinical features and laboratory findings (the overgrowth syndrome, red hair, hypoglycemia and hypocortisolism) the patient was diagnosed as POMC deficiency and the diagnosis was confirmed by genetic studies. Hypoglycemia and apnea episodes ceased as he was put on hydrocortisone but he developed relative mineralocorticoid deficiency during a urinary tract infection. In POMC deficiency, relative mineralocorticoid deficiency should be in mind in episodes of severe stress and therapy should be initiated.
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