Search on: PIEBALDISM 
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Descriptor English:   Piebaldism 
Descriptor Spanish:   Piebaldismo 
Descriptor Portuguese:   Piebaldismo 
Synonyms English:   Albinism, Cutaneous
Albinism, Partial  
Tree Number:   C16.320.290.040.600
C16.320.565.100.102.600
C16.320.850.080.600
C17.800.621.440.102.600
C17.800.827.080.600
C18.452.648.100.102.600
Definition English:   Autosomal dominant, congenital disorder characterized by localized hypomelanosis of the skin and hair. The most familiar feature is a white forelock presenting in 80 to 90 percent of the patients. The underlying defect is possibly related to the differentiation and migration of melanoblasts, as well as to defective development of the neural crest (neurocristopathy). Piebaldism may be closely related to WAARDENBURG SYNDROME. 
Indexing Annotation English:   hypopigmentation of skin & hair; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
See Related English:   Waardenburg Syndrome
 
History Note English:   91 
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:   29082 
Unique Identifier:   D016116 

Occurrence in VHL:
 

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