Tags

Type your tag names separated by a space and hit enter

Heart-hand syndrome II. A report of Tabatznik syndrome with new findings.
Clin Genet. 1990 Aug; 38(2):105-13.CG

Abstract

The association of upper limb malformations and congenital cardiac anomalies was established as a definite clinical and genetic entity by Holt & Oram in 1960. Significant variability of malformations in both the upper limbs and the cardiovascular system has been well documented. In 1978, Temtamy & McKusick reported a family studied by Tabatznik, in which upper limb deformities, including type D brachydactyly, occurred in association with cardiac arrhythmias as a dominant, either autosomal or X-linked trait. They called this apparently new entity "Heart-Hand syndrome II" to distinguish it from the Holt-Oram syndrome. No other similar cases have subsequently been reported. We describe here the second family affected with the Tabatznik syndrome and add some new findings to the clinical spectrum of this condition.

Authors+Show Affiliations

Istituto di Discipline Pediatriche, Servizio de Genetiea Clinica, Universita'di Torino, Italy.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

1976459

Citation

Silengo, M C., et al. "Heart-hand Syndrome II. a Report of Tabatznik Syndrome With New Findings." Clinical Genetics, vol. 38, no. 2, 1990, pp. 105-13.
Silengo MC, Biagioli M, Guala A, et al. Heart-hand syndrome II. A report of Tabatznik syndrome with new findings. Clin Genet. 1990;38(2):105-13.
Silengo, M. C., Biagioli, M., Guala, A., Lopez-Bell, G., & Lala, R. (1990). Heart-hand syndrome II. A report of Tabatznik syndrome with new findings. Clinical Genetics, 38(2), 105-13.
Silengo MC, et al. Heart-hand Syndrome II. a Report of Tabatznik Syndrome With New Findings. Clin Genet. 1990;38(2):105-13. PubMed PMID: 1976459.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Heart-hand syndrome II. A report of Tabatznik syndrome with new findings. AU - Silengo,M C, AU - Biagioli,M, AU - Guala,A, AU - Lopez-Bell,G, AU - Lala,R, PY - 1990/8/1/pubmed PY - 1990/8/1/medline PY - 1990/8/1/entrez SP - 105 EP - 13 JF - Clinical genetics JO - Clin Genet VL - 38 IS - 2 N2 - The association of upper limb malformations and congenital cardiac anomalies was established as a definite clinical and genetic entity by Holt & Oram in 1960. Significant variability of malformations in both the upper limbs and the cardiovascular system has been well documented. In 1978, Temtamy & McKusick reported a family studied by Tabatznik, in which upper limb deformities, including type D brachydactyly, occurred in association with cardiac arrhythmias as a dominant, either autosomal or X-linked trait. They called this apparently new entity "Heart-Hand syndrome II" to distinguish it from the Holt-Oram syndrome. No other similar cases have subsequently been reported. We describe here the second family affected with the Tabatznik syndrome and add some new findings to the clinical spectrum of this condition. SN - 0009-9163 UR - https://www.unboundmedicine.com/medline/citation/1976459/Heart_hand_syndrome_II__A_report_of_Tabatznik_syndrome_with_new_findings_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0009-9163&date=1990&volume=38&issue=2&spage=105 DB - PRIME DP - Unbound Medicine ER -