Cantu syndrome in an Egyptian child
Joint Authors
Source
The Egyptian Journal of Medical Human Genetics
Issue
Vol. 19, Issue 4 (31 Oct. 2018), pp.429-432, 4 p.
Publisher
Egyptian Society of Human Genetics
Publication Date
2018-10-31
Country of Publication
Egypt
No. of Pages
4
Main Subjects
Topics
Abstract EN
We report a 3 month old female, third in order of birth of non consanguineous Egyptian parents with the typical features of Cantu syndrome including coarse features, low frontal hairline, hairy forehead, broad flat nasal bridge, anteverted nares, long philtrum, small low set ears, high arched palate, excess hair on the cheeks, short neck and excess hair over extremities and back.
The patient had patent ductus arteriosus ligation, and mild pulmonary hypertension.
Our patient has an affected mother which is consistent with autosomal dominant inheritance.
American Psychological Association (APA)
Shawqi, Rabah M.& Jamal, Radwah. 2018. Cantu syndrome in an Egyptian child. The Egyptian Journal of Medical Human Genetics،Vol. 19, no. 4, pp.429-432.
https://search.emarefa.net/detail/BIM-902682
Modern Language Association (MLA)
Shawqi, Rabah M.& Jamal, Radwah. Cantu syndrome in an Egyptian child. The Egyptian Journal of Medical Human Genetics Vol. 19, no. 4 (Oct. 2018), pp.429-432.
https://search.emarefa.net/detail/BIM-902682
American Medical Association (AMA)
Shawqi, Rabah M.& Jamal, Radwah. Cantu syndrome in an Egyptian child. The Egyptian Journal of Medical Human Genetics. 2018. Vol. 19, no. 4, pp.429-432.
https://search.emarefa.net/detail/BIM-902682
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 432
Record ID
BIM-902682