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bn:03430533n
Noun Concept
SYL
No term available
EN
Pierre Robin sequence is a congenital defect observed in humans which is characterized by facial abnormalities. Wikipedia
Relations
Sources
IS A
EN
disease
EN
sequence
EN
First arch syndrome
HAS KIND
EN
Weissenbacher-Zweymuller syndrome
EN
Catel–Manzke syndrome
HEALTH SPECIALTY
EN
medical genetics
NAMED AFTER
Pierre Robin
SYMPTOMS
EN
glossoptosis

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