[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.
MeSH
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 -