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Allgrove Syndrome: Adrenal Insufficiency with Hypertensive Encephalopathy.
Author(s):
1. Sommayya Aftab: Department of Paediatric Endocrinology, The Children's Hospital and ICH, Lahore, Pakistan
2. Jaida Manzoor: Department of Paediatric Endocrinology, The Children's Hospital and ICH, Lahore, Pakistan
3. Nabila Talat: Department of Paediatric Surgery, The Children's Hospital and ICH, Lahore, Pakistan
4. Hafiz Sajid Khan: Department of Paediatric Endocrinology, The Children's Hospital and ICH, Lahore, Pakistan
5. Maroof Subhanie: Department of Paediatric Endocrinology, The Children's Hospital and ICH, Lahore, Pakistan
6. Nauman Abbas Khalid: Department of Paediatric Endocrinology, The Children's Hospital and ICH, Lahore, Pakistan
Abstract:
Allgrove syndrome or triple-A syndrome is a rare familial multisystem autosomal recessive disorder. It is characterised by triad of alacrima, achalasia and adrenal insufficiency due to adrenocorticotropin hormone (ACTH) resistance. If it is associated with autonomic dysfunction, it is termed as 4-A syndrome. This syndrome is caused by a mutation in the Achalasia - Addisonism - Alacrima (AAAS) gene on chromosome 12q13 encoding the nuclear pore protein ALADIN. A 5-year boy presented with history of fits and altered sensorium for one day. He also had increased pigmentation of body and persistent vomiting since six months of age. Laboratory investigations and imaging revealed alacrimia, achalasia and adrenal insufficiency due to ACTH resistance. He had episodes of hypertensive crises, for which he was thoroughly investigated and it was found to be due to autonomic instability. Based on clinical findings and investigations he was diagnosed as case of Allgrove syndrome or 4-A syndrome with autonomic dysfunction.
Page(s): 790-792
DOI: DOI not available
Published: Journal: Journal of College of Physicians and Surgeons--Pakistan : JCPSP, Volume: 26, Issue: 9, Year: 2016
Keywords:
Achalasia Alacrima Adrenal insufficiency TripleA syndrome Allgrove syndrome Hypertension Autonomic dysfunction
References:
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[6] PatersonWG, 2001.Etiology and pathogenesis of achalasia,Gastrointest Endosc Clin N Am 11 249 -66
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