serw-MX  [xml]  
 


    
 DeCS Categories

C05 Musculoskeletal Diseases .
C05.500 Jaw Diseases .
C05.500.460 Jaw Abnormalities .
C05.500.460.606 Pierre Robin Syndrome .
C05.660 Musculoskeletal Abnormalities .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.540 Maxillofacial Abnormalities .
C05.660.207.540.460 Jaw Abnormalities .
C05.660.207.540.460.606 Pierre Robin Syndrome .
C07 Stomatognathic Diseases .
C07.320 Jaw Diseases .
C07.320.440 Jaw Abnormalities .
C07.320.440.606 Pierre Robin Syndrome .
C07.650 Stomatognathic System Abnormalities .
C07.650.500 Maxillofacial Abnormalities .
C07.650.500.460 Jaw Abnormalities .
C07.650.500.460.606 Pierre Robin Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.207 Craniofacial Abnormalities .
C16.131.621.207.540 Maxillofacial Abnormalities .
C16.131.621.207.540.460 Jaw Abnormalities .
C16.131.621.207.540.460.606 Pierre Robin Syndrome .
C16.131.850 Stomatognathic System Abnormalities .
C16.131.850.500 Maxillofacial Abnormalities .
C16.131.850.500.460 Jaw Abnormalities .
C16.131.850.500.460.606 Pierre Robin Syndrome .
Z01 Geographic Locations .
Z01.542 Europe .
Z01.542.286 France .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
France .
Miquelon and Saint Pierre .
Miquelon and St. Pierre .
St. Pierre and Miquelon .
Corsica .
Saint Pierre and Miquelon .
A country in western Europe bordered by the Atlantic Ocean, the English Channel, the Mediterranean Sea, and the countries of Belgium, Germany, Italy, Spain, Switzerland, the principalities of Andorra and Monaco, and by the duchy of Luxembourg. Its capital is Paris. .
1.00
26283150
 
Pierre Robin Syndrome .
Glossoptosis, Micrognathia, and Cleft Palate .
Pierre Robin Sequence .
Pierre Robin's Sequence .
Pierre-Robin Syndrome .
Robin Sequence .
Pierre Robins Sequence .
Robin Syndrome, Pierre .
Sequence, Pierre Robin .
Sequence, Pierre Robin's .
Sequence, Robin .
Syndrome, Pierre Robin .
Syndrome, Pierre-Robin .
Congenital malformation characterized by MICROGNATHIA or RETROGNATHIA; GLOSSOPTOSIS and CLEFT PALATE. The mandibular abnormalities often result in difficulties in sucking and swallowing. The syndrome may be isolated or associated with other syndromes (e.g., ANDERSEN SYNDROME; CAMPOMELIC DYSPLASIA). Developmental mis-expression of SOX9 TRANSCRIPTION FACTOR gene on chromosome 17q and its surrounding region is associated with the syndrome. .
0.36
551149