Freeman-Sheldon syndrome: a case report.Quintessence Int. 2003 Apr; 34(4):307-10.QI
Abstract
Freeman-Sheldon syndrome, also called "whistling-face syndrome," is a very rare genetic condition, occurring both sporadically and by transmission through autosomal dominant or recessive mode, which affects primarily the face and skeleton. Characteristics include microstomia of the mouth, which gives the person a whistling appearance, a flat face, club feet, contracted joint muscles of the fingers and hands, and underdeveloped nose cartilage. This article describes a case of Freeman-Sheldon syndrome in a 10-year-old male. The most apparent deformities are associated with orofacial and skeletal development.
MeSH
Pub Type(s)
Case Reports
Journal Article
Language
eng
PubMed ID
12731619
Citation
Aren, Gamze, et al. "Freeman-Sheldon Syndrome: a Case Report." Quintessence International (Berlin, Germany : 1985), vol. 34, no. 4, 2003, pp. 307-10.
Aren G, Yurdabakan Z, Ozcan I. Freeman-Sheldon syndrome: a case report. Quintessence Int. 2003;34(4):307-10.
Aren, G., Yurdabakan, Z., & Ozcan, I. (2003). Freeman-Sheldon syndrome: a case report. Quintessence International (Berlin, Germany : 1985), 34(4), 307-10.
Aren G, Yurdabakan Z, Ozcan I. Freeman-Sheldon Syndrome: a Case Report. Quintessence Int. 2003;34(4):307-10. PubMed PMID: 12731619.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Freeman-Sheldon syndrome: a case report.
AU - Aren,Gamze,
AU - Yurdabakan,Zuhal,
AU - Ozcan,Ilknur,
PY - 2003/5/7/pubmed
PY - 2003/7/2/medline
PY - 2003/5/7/entrez
SP - 307
EP - 10
JF - Quintessence international (Berlin, Germany : 1985)
JO - Quintessence Int
VL - 34
IS - 4
N2 - Freeman-Sheldon syndrome, also called "whistling-face syndrome," is a very rare genetic condition, occurring both sporadically and by transmission through autosomal dominant or recessive mode, which affects primarily the face and skeleton. Characteristics include microstomia of the mouth, which gives the person a whistling appearance, a flat face, club feet, contracted joint muscles of the fingers and hands, and underdeveloped nose cartilage. This article describes a case of Freeman-Sheldon syndrome in a 10-year-old male. The most apparent deformities are associated with orofacial and skeletal development.
SN - 0033-6572
UR - https://www.unboundmedicine.com/medline/citation/12731619/Freeman_Sheldon_syndrome:_a_case_report_
L2 - http://www.diseaseinfosearch.org/result/2921
DB - PRIME
DP - Unbound Medicine
ER -