Document Detail


Variable expression of clinical features of Martin Bell syndrome in younger patients.
MedLine Citation:
PMID:  7875865     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The clinical features of 20 patients of Martin Bell syndrome were analyzed in order to derive diagnostic features in younger patients. The characteristic clinical features comprising long face, large ears and macro-orchidism were commoner in children more than 10 years old than in prepubertal children. This study shows that younger the patient, fewer the classical features exhibited. Hyperactivity was the most useful feature for diagnosis of the younger patient with Martin Bell syndrome.
Authors:
I C Verma; R Elango
Related Documents :
12098655 - Impaired nocturnal synthesis of melatonin in patients with cardiac syndrome x.
7063695 - 99mtc-hida cholescintigraphy in dubin-johnson and rotor syndromes.
20472505 - Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (digeorge sy...
20149055 - Endometriosis in a patient with rokitansky-kuster-hauser syndrome.
18594275 - Work-up and management of paediatric cushing's syndrome.
1096555 - Induction of physical dependence upon alcohol in nonhuman primates.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Indian pediatrics     Volume:  31     ISSN:  0019-6061     ISO Abbreviation:  Indian Pediatr     Publication Date:  1994 Apr 
Date Detail:
Created Date:  1995-04-06     Completed Date:  1995-04-06     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  2985062R     Medline TA:  Indian Pediatr     Country:  INDIA    
Other Details:
Languages:  eng     Pagination:  433-8     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, All India Institute of Medical Sciences, New Delhi.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Age Factors
Child
Child Behavior Disorders / etiology
Child, Preschool
Chromosome Aberrations / genetics
Chromosome Disorders
Female
Fragile X Syndrome / complications,  diagnosis*,  genetics
Humans
Male
Mental Retardation / etiology

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Socio-economic burden of childhood asthma.
Next Document:  Reversal of clinical and dental fluorosis.