Search on:
PIERRE ROBIN SYNDROME
Descriptors Found:
1
Displaying:
1 .. 1
1 / 1
DeCS
Descriptor
English
:
Pierre Robin Syndrome
Descriptor
Spanish
:
Síndrome de Pierre Robin
Descriptor
Portuguese
:
Síndrome de Pierre Robin
Tree Number:
C05.500.460.606
C05.660.207.540.460.606
C07.320.440.606
C07.650.500.460.606
C16.131.621.207.540.460.606
C16.131.850.500.460.606
Definition
English
:
An autosomal recessive disorder characterized by brachygnathia and
cleft palate
, often associated with glossoptosis, backward and upward displacement of the
larynx
, and angulation of the
manubrium
sterni.
Cleft palate
makes sucking and swallowing difficult, permitting easy access of fluids into the
larynx
. It may appear in several syndromes or as an isolated hypoplasia. (Dorland, 27th ed)
Indexing Annotation
English
:
multiple oral abnorm; named for French dentist Pierre Robin: Robin is his surname; note: no hyphen; do not use /congen & do not coord with
INFANT
, NEWBORN, DISEASES
History Note
English
:
65(64)
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:
11288
Unique Identifier:
D010855
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
LIS