Literature DB >> 1655458

Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders.

M Dumić1, A Radica, Z Sabol, V Plavsić, L Brkljacić, V Sarnavka, J Vuković.   

Abstract

Five children with adrenocorticotropic hormone (ACTH) insensitivity associated with autonomic nervous system disorders are described. At the time of diagnosis, four of them had osteoporosis. The fifth patient died and skeletal roentgenograms were not done. Osteoporosis was subsequently discovered in one of our previously reported patients with ACTH insensitivity. We assume that osteoporosis is, at least partly, the result of decreased adrenal androgen production. Human leucocyte antigen typing failed to establish any linkage.

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Year:  1991        PMID: 1655458     DOI: 10.1007/bf01958757

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  11 in total

1.  Selective ACTH insensitivity associated with autonomic nervous system disorders and sensory polyneuropathy.

Authors:  M Dumić; A Radica; A Jusić; N Stefanović; Z Murko
Journal:  Eur J Pediatr       Date:  1987-11       Impact factor: 3.183

2.  Hereditary adrenocortical unresponsiveness to adrenocorticotropic hormone.

Authors:  R P Kelch; S L Kaplan; E G Biglieri; G H Daniels; C J Epstein; M M Grumbach
Journal:  J Pediatr       Date:  1972-10       Impact factor: 4.406

3.  Ocular and fingertip abnormalities in isolated glucocorticoid deficiency.

Authors:  R Counahan; R West
Journal:  J Pediatr       Date:  1974-10       Impact factor: 4.406

4.  The distribution of HL-A antigens and genes in the Yugoslav population.

Authors:  A Kastelan; V Kerhin-Brkljacić; J Hors; L Brkljacić; P Maćasović
Journal:  Tissue Antigens       Date:  1974

5.  Bone mineral density in Addison's disease.

Authors:  R G Crilly
Journal:  Br Med J (Clin Res Ed)       Date:  1987-06-06

6.  Selective ACTH insensitivity, achalasia, and alacrima: a multisystem disorder presenting in childhood.

Authors:  M E Geffner; B M Lippe; S A Kaplan; W E Berquist; J B Bateman; V I Paterno; R Seegan
Journal:  Pediatr Res       Date:  1983-07       Impact factor: 3.756

7.  Adrenalectomy of rats results in hypomyelination of the central nervous system.

Authors:  S L Preston; F A McMorris
Journal:  J Neurochem       Date:  1984-01       Impact factor: 5.372

8.  Glucocorticoid and partial mineralocorticoid deficiency associated with achalasia.

Authors:  R Lanes; L P Plotnick; T E Bynum; P A Lee; J F Casella; C E Fox; A A Kowarski; C J Migeon
Journal:  J Clin Endocrinol Metab       Date:  1980-02       Impact factor: 5.958

9.  Bone mineral density in Addison's disease: evidence for an effect of adrenal androgens on bone mass.

Authors:  J P Devogelaer; J Crabbé; C Nagant de Deuxchaisnes
Journal:  Br Med J (Clin Res Ed)       Date:  1987-03-28

10.  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

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  10 in total

1.  Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.

Authors:  Miroslav Dumic; Nina Barišic; Vesna Kusec; Katarina Stingl; Mate Skegro; Andrija Stanimirovic; Katrin Koehler; Angela Huebner
Journal:  Eur J Pediatr       Date:  2012-04-28       Impact factor: 3.183

2.  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

3.  Intracellular ROS level is increased in fibroblasts of triple A syndrome patients.

Authors:  Barbara Kind; Katrin Koehler; Manuela Krumbholz; Dana Landgraf; Angela Huebner
Journal:  J Mol Med (Berl)       Date:  2010-08-13       Impact factor: 4.599

4.  Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy.

Authors:  Miroslav Dumić; Nina Barišić; Nataša Rojnić-Putarek; Vesna Kušec; Andrija Stanimirović; Katrin Koehler; Angela Huebner
Journal:  Eur J Pediatr       Date:  2010-10-08       Impact factor: 3.183

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

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.  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

8.  Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiology.

Authors:  M Dumic; N R Putarek; V Kusec; N Barisic; K Koehler; A Huebner
Journal:  Osteoporos Int       Date:  2015-08-05       Impact factor: 4.507

9.  Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome.

Authors:  Alma Toromanovic; Husref Tahirovic; Tatjana Milenkovic; Katrin Koehler; Barbara Kind; Dragan Zdravkovic; Mensuda Hasanhodzic; Angela Huebner
Journal:  Eur J Pediatr       Date:  2008-06-13       Impact factor: 3.183

10.  Longitudinal neuropsychological profile in a patient with triple a syndrome.

Authors:  Luigi Mazzone; Valentina Postorino; Lavinia De Peppo; Lia Vassena; Laura Fatta; Marco Armando; Giuseppe Scirè; Marco Cappa; Stefano Vicari
Journal:  Case Rep Pediatr       Date:  2013-04-09
  10 in total

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