Pierre Robin Syndrome [Pierre Robinův syndrom]
- Terms
-
sekvence Pierre Robinova
-
Glossoptosis, Micrognathia, and Cleft Palate
Pierre Robin Sequence
Pierre Robin's Sequence
Pierre-Robin Syndrome
Robin Sequence
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.
- Annotation
- named for French dentist Pierre Robin: Robin is his surname; note: no hyphen
- název po francouzském stomatologovi Pierru Robinovi; bez pomlčky
- DUI
- D010855 MeSH Browser
- CUI
- M0016846
- History note
- 65(64)
- Public note
- 65
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 5
- DI
- diagnosis 5
- DG
- diagnostic imaging 1
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology 1
- EN
- enzymology
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 3
- GE
- genetics 2
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing 1
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 2
- TH
- therapy 5
- UR
- urine
- VE
- veterinary
- VI
- virology
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Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence Disease MeSH Browser
Femoral facial syndrome Disease MeSH Browser
Myopathy, congenital nonprogressive with Moebius and Robin sequences Disease MeSH Browser
Pierre Robin Sequence with Facial and Digital Anomalies Disease MeSH Browser
Pierre Robin sequence with pectus excavatum and rib and scapular anomalies Disease MeSH Browser
Pierre Robin syndrome with fetal chondrodysplasia Disease MeSH Browser
Radial defect Robin sequence Disease MeSH Browser
Richieri Costa Pereira syndrome Disease MeSH Browser
Robin Sequence with Distinctive Facial Appearance and Brachydactyly Disease MeSH Browser
Robin sequence and oligodactyly Disease MeSH Browser
Sanderson Fraser syndrome Disease MeSH Browser
Stevenson-Carey Syndrome Disease MeSH Browser
Stoll Alembik Dott syndrome Disease MeSH Browser
TARP syndrome Disease MeSH Browser
Thrombocytopenia Robin sequence Disease MeSH Browser
Ventricular extrasystoles perodactyly Robin sequence Disease MeSH Browser