Literature DB >> 26354489

Allgrove (Triple A) Syndrome: A Case Report from the Kashmir Valley.

Raiz Ahmad Misgar1, Nazir Ahmad Pala2, Mahroosa Ramzan2, Arshad Iqbal Wani2, Mir Iftikhar Bashir2, Bashir Ahmad Laway2.   

Abstract

Allgrove (Triple A) syndrome is a rare autosomal recessive disorder characterized by cardinal features of adrenal insufficiency due to adrenocorticotropic hormone (ACTH) resistance, achalasia, and alacrimia. It is frequently associated with neurological manifestations like polyneuropathy. Since its first description by Allgrove in 1978, approximately 100 cases have been reported in the literature. Here we report an 18-year-old boy diagnosed as having Allgrove syndrome, with ACTH resistant adrenal insufficiency, achalasia, alacrimia, and severe motor polyneuropathy. Alacrimia was the earliest feature evident at the age of 8 years. He presented with achalasia and adrenal insufficiency at 12 and 18 years respectively and developed neurological symptoms in the form of severe muscle wasting at the age of 15 years. Patients with Allgrove syndrome usually manifest adrenal insufficiency and achalasia during first decade of life. Our patient manifested adrenal insufficiency and achalasia in the second decade and manifested neurological dysfunction before adrenal dysfunction.

Entities:  

Keywords:  Adrenal insufficiency; Alacrimia; Polyneuropathies

Year:  2015        PMID: 26354489      PMCID: PMC4722417          DOI: 10.3803/EnM.2015.30.4.604

Source DB:  PubMed          Journal:  Endocrinol Metab (Seoul)        ISSN: 2093-596X


  8 in total

1.  Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation.

Authors:  C Goizet; B Catargi; F Tison; A Tullio-Pelet; S Hadj-Rabia; F Pujol; A Lagueny; S Lyonnet; D Lacombe
Journal:  Neurology       Date:  2002-03-26       Impact factor: 9.910

Review 2.  Adrenocorticotropin insensitivity syndromes.

Authors:  A J Clark; A Weber
Journal:  Endocr Rev       Date:  1998-12       Impact factor: 19.871

3.  Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster.

Authors:  A Weber; T F Wienker; M Jung; D Easton; H J Dean; C Heinrichs; A Reis; A J Clark
Journal:  Hum Mol Genet       Date:  1996-12       Impact factor: 6.150

4.  Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropin.

Authors:  F Sandrini; C Farmakidis; L S Kirschner; S M Wu; A Tullio-Pelet; S Lyonnet; D L Metzger; C J Bourdony; D Tiosano; W Y Chan; C A Stratakis
Journal:  J Clin Endocrinol Metab       Date:  2001-11       Impact factor: 5.958

5.  Two cases of Allgrove syndrome with mutations in the AAAS gene.

Authors:  Saori Kinjo; Megumi Takemoto; Kenichi Miyako; Hitoshi Kohno; Toshiaki Tanaka; Noriyuki Katsumata
Journal:  Endocr J       Date:  2004-10       Impact factor: 2.349

6.  Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome.

Authors:  D B Grant; N D Barnes; M Dumic; M Ginalska-Malinowska; P J Milla; W von Petrykowski; R J Rowlatt; R Steendijk; J H Wales; E Werder
Journal:  Arch Dis Child       Date:  1993-06       Impact factor: 3.791

7.  Variant of the Triple A syndrome.

Authors:  P L Khong; W C Peh; L C Low; L L Leong
Journal:  Australas Radiol       Date:  1994-08

8.  Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production.

Authors:  J Allgrove; G S Clayden; D B Grant; J C Macaulay
Journal:  Lancet       Date:  1978-06-17       Impact factor: 79.321

  8 in total
  3 in total

1.  Clinical and genetic characterisation of a series of patients with triple A syndrome.

Authors:  Erdal Kurnaz; Paolo Duminuco; Zehra Aycan; Şenay Savaş-Erdeve; Nursel Muratoğlu Şahin; Melişah Keskin; Elvan Bayramoğlu; Marco Bonomi; Semra Çetinkaya
Journal:  Eur J Pediatr       Date:  2017-12-19       Impact factor: 3.183

2.  Allgrove syndrome and motor neuron disease.

Authors:  Marcos R G de Freitas; Marco Orsini; Alexandra Prufer de Queiroz Campos Araújo; Luiz João Abraão; Gilberto Miranda Barbosa; Marcondes C França; Luan Correia; Victor Hugo Bastos; Eduardo Trajano; Mauricio da Sant'Anna
Journal:  Neurol Int       Date:  2018-07-04

3.  Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report.

Authors:  H Berrani; T Meskini; M Zerkaoui; H Merhni; S Ettair; A Sefiani; N Mouane
Journal:  BMC Pediatr       Date:  2018-06-04       Impact factor: 2.125

  3 in total

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