Document Detail


The neurogenetics of mucolipidosis type IV.
MedLine Citation:
PMID:  12182165     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Mucolipidosis type IV (MLIV) is an autosomal recessive disease caused by mutations in the MCOLN1 gene that codes for mucolipin, a member of the transient receptor potential (TRP) gene family. OBJECTIVE: To comprehensively characterize the clinical and genetic abnormalities of MLIV. METHODS: Twenty-eight patients with MLIV, aged 2 to 25 years, were studied. Ten returned for follow-up every 1 to 2 years for up to 5 years. Standard clinical, neuroimaging, neurophysiologic, and genetic techniques were used. RESULTS: All patients had varying degrees of corneal clouding, with progressive optic atrophy and retinal dystrophy. Twenty-three patients had severe motor and mental impairment. Motor function deteriorated in three patients and remained stable in the rest. All had a constitutive achlorhydria with elevated plasma gastrin level, and 12 had iron deficiency or anemia. Head MRI showed consistent characteristic findings of a thin corpus callosum and remained unchanged during the follow-up period. Prominent abnormalities of speech, hand usage, and swallowing were also noted. Mutations in the MCOLN1 gene were present in all patients. Correlation of the genotype with the neurologic handicap and corpus callosum dysplasia was found. CONCLUSIONS: MLIV is both a developmental and a degenerative disorder. The presentation as a cerebral palsy-like encephalopathy may delay diagnosis.
Authors:
G Altarescu; M Sun; D F Moore; J A Smith; E A Wiggs; B I Solomon; N J Patronas; K P Frei; S Gupta; C R Kaneski; O W Quarrell; S A Slaugenhaupt; E Goldin; R Schiffmann
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Neurology     Volume:  59     ISSN:  0028-3878     ISO Abbreviation:  Neurology     Publication Date:  2002 Aug 
Date Detail:
Created Date:  2002-08-15     Completed Date:  2002-09-03     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0401060     Medline TA:  Neurology     Country:  United States    
Other Details:
Languages:  eng     Pagination:  306-13     Citation Subset:  AIM; IM    
Affiliation:
Developmental and Metabolic Neurology Branch, National Institute of Neurologic Disorders and Stroke/NIH, 9000 Rockville Pike, Building 10, Rm. 3D03, Bethesda, MD 20892-1260, USA.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Child
Child, Preschool
Corpus Callosum / pathology
Diagnosis, Differential
Electroencephalography
Female
Follow-Up Studies
Genotype
Humans
Male
Membrane Proteins / chemistry,  genetics*
Mucolipidoses / diagnosis,  genetics*,  pathology,  physiopathology*
Mutation / genetics
Phenotype
Prospective Studies
TRPM Cation Channels
Grant Support
ID/Acronym/Agency:
NS 39995/NS/NINDS NIH HHS
Chemical
Reg. No./Substance:
0/MCOLN1 protein, human; 0/Membrane Proteins; 0/TRPM Cation Channels

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


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