Search on: MANDIBULOFACIAL DYSOSTOSIS 
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Descriptor English:   Mandibulofacial Dysostosis 
Descriptor Spanish:   Disostosis Mandibulofacial 
Descriptor Portuguese:   Disostose Mandibulofacial 
Synonyms English:   Treacher Collins Syndrome  
Tree Number:   C05.116.099.370.231.576
C05.660.207.231.576
C16.131.621.207.231.576
Definition English:   A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed) 
Indexing Annotation English:   a form of craniofacial dysostosis; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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:   8514 
Unique Identifier:   D008342 

Occurrence in VHL:
 

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