Holt-Oram Syndrome

Hamiyet Pekel, Hidayet Durmaz

  • Year : 1989
  • Vol : 5
  • No : 2
  •  Page : 147-150
A maIe child who had a skeletal and cardiovascular anomaly relaled with Synrome and esotropia was presented. On !his palient following symptoms were observed; bilaterally hypoplasique arm, 3 fingers on the right and 4 flngers on the left hand, arrioseptal defect and on the. eye 35 prisin diopri esoıropia, in the pedigri, tl was stated that was a first mutation occurred in mother.
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
Holt-Oram Syndrome
, Vol. 5 (2)
Received : 23.11.1989, Accepted : 23.11.1989, Published Online : 23.11.2020
Selçuk Tıp Dergisi
ISSN:1017-6616;
E-ISSN:2149-8059;
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