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Additional case of Keipert syndrome and review of the literature.
Med Sci Monit. 2000 Jul-Aug; 6(4):776-8.MS

Abstract

We report on a 7-year-old boy with unusual facial features, severe bilateral sensorineural hearing loss, and broad terminal phalanges. These findings are similar to those described by Keipert et al. in two brothers and by Balci and Dagli in two other male siblings. Our patient has, in addition, developmental delay and abnormal behaviour. To the best of our knowledge, this is only the third report of Keipert syndrome.

Authors+Show Affiliations

Department of Paediatrics, Queen's University and Kingston General Hospital, Kingston, Canada.No affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

11208408

Citation

Cappon, S M., and M M. Khalifa. "Additional Case of Keipert Syndrome and Review of the Literature." Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, vol. 6, no. 4, 2000, pp. 776-8.
Cappon SM, Khalifa MM. Additional case of Keipert syndrome and review of the literature. Med Sci Monit. 2000;6(4):776-8.
Cappon, S. M., & Khalifa, M. M. (2000). Additional case of Keipert syndrome and review of the literature. Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 6(4), 776-8.
Cappon SM, Khalifa MM. Additional Case of Keipert Syndrome and Review of the Literature. Med Sci Monit. 2000 Jul-Aug;6(4):776-8. PubMed PMID: 11208408.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Additional case of Keipert syndrome and review of the literature. AU - Cappon,S M, AU - Khalifa,M M, PY - 2001/2/24/pubmed PY - 2001/4/6/medline PY - 2001/2/24/entrez SP - 776 EP - 8 JF - Medical science monitor : international medical journal of experimental and clinical research JO - Med. Sci. Monit. VL - 6 IS - 4 N2 - We report on a 7-year-old boy with unusual facial features, severe bilateral sensorineural hearing loss, and broad terminal phalanges. These findings are similar to those described by Keipert et al. in two brothers and by Balci and Dagli in two other male siblings. Our patient has, in addition, developmental delay and abnormal behaviour. To the best of our knowledge, this is only the third report of Keipert syndrome. SN - 1234-1010 UR - https://www.unboundmedicine.com/medline/citation/11208408/Additional_case_of_Keipert_syndrome_and_review_of_the_literature_ L2 - https://www.medscimonit.com/download/index/idArt/508215 DB - PRIME DP - Unbound Medicine ER -