Literature DB >> 3565479

Familial achalasia associated with adrenocortical insufficiency, alacrima, and neurological abnormalities.

E Ehrich, G Aranoff, W G Johnson.   

Abstract

We report on two brothers with achalasia, adrenocortical insufficiency, alacrima, short stature, microcephaly, ataxia, optic atrophy, and developmental delay. The parents and three sibs are unaffected. Achalasia, adrenocortical insufficiency, and alacrima comprise a recently characterized familial multisystem disorder of unknown cause. Achalasia has also been described in association with microcephaly and mental retardation in one family and ataxia, optic atrophy, and mental retardation in another. The above reports and these sibs may represent variants of a single pleiotropic recessive gene. We suggest that abnormalities of the central nervous system are a manifestation of the achalasia, adrenocortical insufficiency, alacrima syndrome.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3565479     DOI: 10.1002/ajmg.1320260319

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  15 in total

1.  New ophthalmic features in a family with triple A syndrome.

Authors:  Marilita M Moschos; Ioannis Margetis; Katrin Koehler; Zisis Gatzioufas; Angela Huebner
Journal:  Int Ophthalmol       Date:  2011-05-28       Impact factor: 2.031

2.  Neurological features in adult Triple-A (Allgrove) syndrome.

Authors:  Anne-Evelyne Vallet; Annie Verschueren; Philippe Petiot; Nadia Vandenberghe; Marc Nicolino; Sabine Roman; Jean Pouget; Christophe Vial
Journal:  J Neurol       Date:  2011-06-09       Impact factor: 4.849

3.  Familial glucocorticoid deficiency, alacrimia and achalasia--Allgrove syndrome.

Authors:  M N Muranjan; M Gurav; T Surve; C T Deshmukh; B A Bharucha
Journal:  Indian J Pediatr       Date:  1999 Jan-Feb       Impact factor: 1.967

4.  Association of adult achalasia and alacrima.

Authors:  S Verma; S Brown; M Dakkak; J R Bennett
Journal:  Dig Dis Sci       Date:  1999-05       Impact factor: 3.199

5.  Familial adrenocorticotropin unresponsiveness associated with alacrima and achalasia: biochemical and molecular studies in two siblings with clinical heterogeneity.

Authors:  C Heinrichs; C Tsigos; J Deschepper; R Drews; R Collu; C Dugardeyn; P Goyens; G E Ghanem; D Bosson; G P Chrousos
Journal:  Eur J Pediatr       Date:  1995-03       Impact factor: 3.183

Review 6.  [Motility disorders of the esophagus].

Authors:  E Bruder; A-L Rougemont; R I Furlano; J F Schneider; J Mayr; F-M Haecker; K Beier; J Schneider; P Weber; T Berberich; G Cathomas; W A Meier-Ruge
Journal:  Pathologe       Date:  2013-03       Impact factor: 1.011

7.  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

8.  The "4A" syndrome: adrenocortical insufficiency associated with achalasia, alacrima, autonomic and other neurological abnormalities.

Authors:  M Gazarian; C T Cowell; M Bonney; W G Grigor
Journal:  Eur J Pediatr       Date:  1995-01       Impact factor: 3.183

9.  Congenital alacrima in a patient with G (Opitz Frias) syndrome.

Authors:  M Dundar; K Erkihç; F Demiryilmaz; M Küçükaydin; M Kendirci; H Okur; A Kazez
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

10.  Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementia.

Authors:  D B Grant; D B Dunger; I Smith; K Hyland
Journal:  Eur J Pediatr       Date:  1992-02       Impact factor: 3.183

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.