Simpson-Golabi-Behmel syndrome associated with cleft palate.J Craniofac Surg. 2011 Sep; 22(5):1917-8.JC
Abstract
We report a very rare case of anomaly in the maxillofacial region. This case is a patient with a cleft palate who had Simpson-Golabi-Behmel syndrome. This X-linked symptom was first described by Simpson et al in 1975 and is characterized by prenatal and postnatal overgrowth, as well as visceral and skeletal anomalies. The syndrome consists of a distinctive facial appearance with wide nasal bridge, anteverted nostrils, wide-open mouth, enlarged tongue, and large protruding maxilla and jaw. The cleft palate was repaired surgically using the push-back method.
Links
MeSH
Pub Type(s)
Case Reports
Journal Article
Language
eng
PubMed ID
21959466
Citation
Morita, Yoshihiro, et al. "Simpson-Golabi-Behmel Syndrome Associated With Cleft Palate." The Journal of Craniofacial Surgery, vol. 22, no. 5, 2011, pp. 1917-8.
Morita Y, Kimoto N, Ogawa H, et al. Simpson-Golabi-Behmel syndrome associated with cleft palate. J Craniofac Surg. 2011;22(5):1917-8.
Morita, Y., Kimoto, N., Ogawa, H., Omata, T., & Morita, N. (2011). Simpson-Golabi-Behmel syndrome associated with cleft palate. The Journal of Craniofacial Surgery, 22(5), 1917-8. https://doi.org/10.1097/SCS.0b013e31822ea73c
Morita Y, et al. Simpson-Golabi-Behmel Syndrome Associated With Cleft Palate. J Craniofac Surg. 2011;22(5):1917-8. PubMed PMID: 21959466.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Simpson-Golabi-Behmel syndrome associated with cleft palate.
AU - Morita,Yoshihiro,
AU - Kimoto,Natsuko,
AU - Ogawa,Hisashi,
AU - Omata,Tetsuji,
AU - Morita,Nobuo,
PY - 2011/10/1/entrez
PY - 2011/10/1/pubmed
PY - 2011/12/30/medline
SP - 1917
EP - 8
JF - The Journal of craniofacial surgery
JO - J Craniofac Surg
VL - 22
IS - 5
N2 - We report a very rare case of anomaly in the maxillofacial region. This case is a patient with a cleft palate who had Simpson-Golabi-Behmel syndrome. This X-linked symptom was first described by Simpson et al in 1975 and is characterized by prenatal and postnatal overgrowth, as well as visceral and skeletal anomalies. The syndrome consists of a distinctive facial appearance with wide nasal bridge, anteverted nostrils, wide-open mouth, enlarged tongue, and large protruding maxilla and jaw. The cleft palate was repaired surgically using the push-back method.
SN - 1536-3732
UR - https://www.unboundmedicine.com/medline/citation/21959466/Simpson_Golabi_Behmel_syndrome_associated_with_cleft_palate_
L2 - https://doi.org/10.1097/SCS.0b013e31822ea73c
DB - PRIME
DP - Unbound Medicine
ER -