Search on: LIPOMUCOPOLYSACCHARIDOSIS 
Descriptors Found: 1
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Descriptor English:   Mucolipidoses 
Descriptor Spanish:   Mucolipidosis 
Descriptor Portuguese:   Mucolipidoses 
Synonyms English:   I-Cell Disease
Lipomucopolysaccharidosis
Pseudo-Hurler Polydystrophy
Cherry Red Spot Myoclonus Syndrome
Ganglioside Sialidase Deficiency Disease
Mucolipidosis
Myoclonus Cherry Red Spot Syndrome
Sialidosis  
Tree Number:   C05.116.198.371
C10.228.140.163.100.435.590
C16.320.565.189.435.590
C16.320.565.202.670
C16.320.565.595.554.590
C18.452.132.100.435.590
C18.452.648.189.435.590
C18.452.648.202.670
C18.452.648.595.554.590
Definition English:   A group of inherited metabolic diseases characterized by the accumulation of excessive amounts of acid mucopolysaccharides, sphingolipids, and/or glycolipids in visceral and mesenchymal cells. Abnormal amounts of sphingolipids or glycolipids are present in neural tissue. INTELLECTUAL DISABILITY and skeletal changes, most notably dysostosis multiplex, occur frequently. (From Joynt, Clinical Neurology, 1992, Ch56, pp36-7) 
See Related English:   Gangliosidoses
 
History Note English:   2000(1977) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   9273 
Unique Identifier:   D009081 

Occurrence in VHL:
 

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