Allgroves's syndrome;Syndrome d'allgrove

Annales de Dermatologie et de Venereologie

Volumn 128, Issue 10 I, 2001, Pages 1043-1045

  Chiheb, S ^a,b   Slaoui, Z ^a   Nejjam, F ^a   Habibeddine, S ^a   Lakhdar, H ^a  

^a IBN ROCHD UNIVERSITY HOSPITAL   (Morocco)

^b Quartier des Hôpitaux   (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROCORTISONE;

ADRENAL INSUFFICIENCY; ALLGROVE SYNDROME; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; ESOPHAGUS ACHALASIA; FAMILY HISTORY; HUMAN; HYPERPIGMENTATION; LACRIMAL GLAND DISEASE; MALE; MELANOMA; PRESCHOOL CHILD; SCHIRMER TEST; SYNDROME DELINEATION;

ADRENAL INSUFFICIENCY; CHILD, PRESCHOOL; DRY EYE SYNDROMES; ESOPHAGEAL ACHALASIA; HUMANS; MALE; MELANOSIS; PEDIGREE; SYNDROME;

EID: 0035183361     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. Familial glucorticoid deficiency with achalasia of the cardia and deficient tear production
2. Coal-blak hyperpigmentation at birth in a child with congenital adrenal hypoplasia
3. Linkage of the gene triple A syndrome to chromosome 12q13 near the type II keratin gene cluster
4. Adrenal insufficiency after achalasia in the triple A syndrome
5. Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasie (3A) syndrome
6. The «4A» syndrome: Adrenocortical insufficiency associated with achalasia, alacrima, autonomic and other neurological abnormalities
7. Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders
8. Familial adrenal insufficiency, achalasia, alacrima, peripheral neuropathy, microcephaly, normal plasma, very long chain fatty acids, and normal muscle mitochondrial respiratory chain enzymes
9. Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementia
10. New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism
11. A microdeletion with DAX-1 in X linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism
12. Congenital adrenal hypoplasia: Clinical spectrum, experience with hormonal diagnosis and report on new point mutations of the DAX-1 gene