Allgrove Syndrome: Case Series on 4A and Triple A Syndrome in Children with Rare Presentation

Medical Journal of Dr. D.Y. Patil Vidyapeeth

article

Roy, Saheli¹  Gupta, Priyanka¹  Basu, Suprit¹  Das, Mrinal K.¹  Datta, Sumana¹ 

[1] Department of Pediatrics, Institute of Postgraduate Medical Education and Research

关键词: 4A;    AAAS gene;    allgrove;    cellulitis;    nephrotic;    orbital;    syndrome;    triple A;   

DOI  :  10.4103/mjdrdypu.mjdrdypu_571_20

学科分类：社会科学、人文和艺术（综合）

来源: Wolters Kluwer Medknow Publications

【 摘 要 】

Introduction:  Allgrove or Triple A syndrome is a rare familial multisystem disorder with autosomal recessive inheritance. Usual features include varied combination of alacrima, achalasia cardia, and adrenocorticotrophic hormone (ACTH) resistant adrenal insufficiency along with autonomic dysfunction and other neurological problems in some cases when it is known as 4A syndrome. Basic defect is in the Achalasia Addisonianism Alacrima Syndrome gene (AAAS) located on chromosome 12q13. Case Details:  This report relates to two unrelated girls aged 7 and 12 years, who presented with orbital cellulitis with acute adrenal crisis and initial episode of nephrotic syndrome, respectively. Both had history of hyperpigmentation of skin, especially palmer creases and knuckles and absence of tear from both eyes while first patient also had autonomic dysfunction. Ophthalmological examination, biochemical evaluations for adrenal function, barium swallow study and magnetic resonance imaging (MRI) of orbits were all consistent with Allgrove Syndrome. Patients were adequately treated for the complications and then put on hormone replacement therapy and ocular lubricants resulting in remarkable improvement on follow up study. Conclusion:  Despite lack of definitive treatment, supportive treatment and hormone replacement can improve quality of life of Allgrove patients.

【 授权许可】

CC BY-NC-SA