Cantu syndrome in an Egyptian child

Joint Authors

Shawqi, Rabah M.
Jamal, Radwah

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

Medicine

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