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[Holt-Oram syndrome. Presentation of two cases (author's transl)].
An Esp Pediatr. 1981 Oct; 15(4):378-82.AE

Abstract

Authors present two new cases of the Host-Oram syndrome in the same family, characterized by the association of cardiac anomalies and the upper members, both aspects varying greatly, transmissible with a dominant autosomal character. In one case there was unilateral renal agenesis, association described for the second time in literature. Data provided by other authors uphold this, as far as the variable and generally progressive penetration of the syndrome are concerned, as well as the frequent association with other diverse malformations.

Authors

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Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

spa

PubMed ID

7337303

Citation

Ferriols Gil, E J., et al. "[Holt-Oram Syndrome. Presentation of Two Cases (author's Transl)]." Anales Espanoles De Pediatria, vol. 15, no. 4, 1981, pp. 378-82.
Ferriols Gil EJ, Fayos Soler JL, Elorza Arizmendi J, et al. [Holt-Oram syndrome. Presentation of two cases (author's transl)]. An Esp Pediatr. 1981;15(4):378-82.
Ferriols Gil, E. J., Fayos Soler, J. L., Elorza Arizmendi, J., & Alvarez Angel, V. (1981). [Holt-Oram syndrome. Presentation of two cases (author's transl)]. Anales Espanoles De Pediatria, 15(4), 378-82.
Ferriols Gil EJ, et al. [Holt-Oram Syndrome. Presentation of Two Cases (author's Transl)]. An Esp Pediatr. 1981;15(4):378-82. PubMed PMID: 7337303.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Holt-Oram syndrome. Presentation of two cases (author's transl)]. AU - Ferriols Gil,E J, AU - Fayos Soler,J L, AU - Elorza Arizmendi,J, AU - Alvarez Angel,V, PY - 1981/10/1/pubmed PY - 1981/10/1/medline PY - 1981/10/1/entrez SP - 378 EP - 82 JF - Anales espanoles de pediatria JO - An Esp Pediatr VL - 15 IS - 4 N2 - Authors present two new cases of the Host-Oram syndrome in the same family, characterized by the association of cardiac anomalies and the upper members, both aspects varying greatly, transmissible with a dominant autosomal character. In one case there was unilateral renal agenesis, association described for the second time in literature. Data provided by other authors uphold this, as far as the variable and generally progressive penetration of the syndrome are concerned, as well as the frequent association with other diverse malformations. SN - 0302-4342 UR - https://www.unboundmedicine.com/medline/citation/7337303/[Holt_Oram_syndrome__Presentation_of_two_cases__author's_transl_]_ L2 - http://www.diseaseinfosearch.org/result/3457 DB - PRIME DP - Unbound Medicine ER -