Journal of Clinical Case Reports

AlAli A

Publications

• Case Report
  Familial Glucocorticoid Deficiency Presenting as Progressive Hyperpigmentation: A Case Report
  Author(s): Refaei A, AlAli A, Soeid M, Jurayyan NA, Alenazi B and Taleb RARefaei A, AlAli A, Soeid M, Jurayyan NA, Alenazi B and Taleb RA
  
  Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disease caused by resistant of ACTH receptor at adrenal cortex leading to (usually) isolated glucocorticoid deficiency with normal mineralocorticoid secrete. Patients with FGD usually presented in neonatal–childhood period with signs/symptoms of glucocorticoid deficiency such as hypoglycemia, hyperpigmentation, Failure to thrive, shock and death if treatment was delayed. Labs usually revealed high ACTH, low cortisol but normal 17 OHP, electrolyte, androgen. Here we describe a 3-yearsold Saudi girl, with history of progressive hyperpigmentation for first year of life, but no history of hypoglycaemia or neonatal jaundice, no history of a lacrimation or dysphagia and positive similar family history. She had generalized Hyperpigmentation with normal female genitalia. Her cortisol was low with high ACTH level, but.. Read More»
  

  Abstract PDF