Aftab Sommayya, Manzoor Jaida, Talat Nabila, Khan Hafiz Sajid, Subhanie Maroof, Khalid Nauman Abbas
Department of Paediatric Endocrinology,The Children's Hospital and ICH, Lahore.
Department of Paediatric Surgery, The Children's Hospital and ICH, Lahore.
J Coll Physicians Surg Pak. 2016 Sep;26(9):790-2.
Allgrove syndrome or triple-Asyndrome 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-Asyndrome. This syndrome is caused by a mutation in the Achalasia - Addisonism - Alacrima (AAAS) gene on chromosome 12q13 encoding the nuclear pore protein ALADIN. A5-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-Asyndrome with autonomic dysfunction.
奥尔格罗夫综合征或三 A 综合征是一种罕见的家族性多系统常染色体隐性疾病。其特征为由于促肾上腺皮质激素(ACTH)抵抗导致的无泪、贲门失弛缓症和肾上腺功能不全三联征。如果伴有自主神经功能障碍,则称为四 A 综合征。该综合征由位于 12q13 染色体上的贲门失弛缓症 - 阿狄森氏病 - 无泪(AAAS)基因突变引起,该基因编码核孔蛋白 ALADIN。一名 5 岁男孩有 1 天的抽搐和意识改变病史。自 6 个月大以来,他还出现了身体色素沉着增加和持续性呕吐。实验室检查和影像学检查显示由于 ACTH 抵抗导致无泪、贲门失弛缓症和肾上腺功能不全。他有高血压危象发作,对此进行了全面检查,发现是由于自主神经不稳定所致。根据临床发现和检查,他被诊断为伴有自主神经功能障碍的奥尔格罗夫综合征或四 A 综合征病例。