Report of a case and further delineation of the SHORT syndrome.Am J Med Genet. 1985 Oct; 22(2):311-4.AJ
Abstract
We describe a boy with the manifestations of the SHORT syndrome: lipoatrophy, delayed speech development, minor facial anomalies, clinodactyly, and short stature. In addition, this boy had deafness, which was not previously reported in the SHORT syndrome.
MeSH
Pub Type(s)
Case Reports
Journal Article
Language
eng
PubMed ID
4050863
Citation
Toriello, H V., et al. "Report of a Case and Further Delineation of the SHORT Syndrome." American Journal of Medical Genetics, vol. 22, no. 2, 1985, pp. 311-4.
Toriello HV, Wakefield S, Komar K, et al. Report of a case and further delineation of the SHORT syndrome. Am J Med Genet. 1985;22(2):311-4.
Toriello, H. V., Wakefield, S., Komar, K., Higgins, J. V., & Waterman, D. F. (1985). Report of a case and further delineation of the SHORT syndrome. American Journal of Medical Genetics, 22(2), 311-4.
Toriello HV, et al. Report of a Case and Further Delineation of the SHORT Syndrome. Am J Med Genet. 1985;22(2):311-4. PubMed PMID: 4050863.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Report of a case and further delineation of the SHORT syndrome.
AU - Toriello,H V,
AU - Wakefield,S,
AU - Komar,K,
AU - Higgins,J V,
AU - Waterman,D F,
PY - 1985/10/1/pubmed
PY - 1985/10/1/medline
PY - 1985/10/1/entrez
SP - 311
EP - 4
JF - American journal of medical genetics
JO - Am J Med Genet
VL - 22
IS - 2
N2 - We describe a boy with the manifestations of the SHORT syndrome: lipoatrophy, delayed speech development, minor facial anomalies, clinodactyly, and short stature. In addition, this boy had deafness, which was not previously reported in the SHORT syndrome.
SN - 0148-7299
UR - https://www.unboundmedicine.com/medline/citation/4050863/Report_of_a_case_and_further_delineation_of_the_SHORT_syndrome_
DB - PRIME
DP - Unbound Medicine
ER -
