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Meningocele in a congolese female with beckwith-wiedemann phenotype.
Mbuyi-Musanzayi S, Lubala Kasole T, Lumaka A, Kayembe Kitenge T, Kabamba Ngombe L, Kalenga Muenze P, Lukusa Tshilobo P, Tshilombo Katombe F, Banza Lubaba Nkulu C, Devriendt K. Mbuyi-Musanzayi S, et al. Among authors: devriendt k. Case Rep Genet. 2014;2014:989425. doi: 10.1155/2014/989425. Epub 2014 Dec 28. Case Rep Genet. 2014. PMID: 25610673 Free PMC article.
Mirror-image gastroschisis in monochorionic female twins.
Lubala TK, Mbuyi-Musanzayi S, Lubala N, Luboya ON, Kalenga PM, Devriendt K, Lukusa-Tshilobo P. Lubala TK, et al. Among authors: devriendt k. Eur J Med Genet. 2015 Apr;58(4):266-9. doi: 10.1016/j.ejmg.2015.03.001. Epub 2015 Mar 14. Eur J Med Genet. 2015. PMID: 25782636
Microtia in Cornelia de Lange syndrome: a case from Democratic Republic of the Congo.
Kayembe Kitenge T, Kasole Lubala T, Mbuyi-Musanzayi S, Kabamba Ngombe L, Katshiez Nawej C, Musa Obadia P, Banza Lubaba Nkulu C, Nemery B, Devriendt K. Kayembe Kitenge T, et al. Among authors: devriendt k. Clin Dysmorphol. 2016 Oct;25(4):178-80. doi: 10.1097/MCD.0000000000000129. Clin Dysmorphol. 2016. PMID: 27088280 No abstract available.
Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator.
Lumaka A, Cosemans N, Lulebo Mampasi A, Mubungu G, Mvuama N, Lubala T, Mbuyi-Musanzayi S, Breckpot J, Holvoet M, de Ravel T, Van Buggenhout G, Peeters H, Donnai D, Mutesa L, Verloes A, Lukusa Tshilobo P, Devriendt K. Lumaka A, et al. Among authors: devriendt k. Clin Genet. 2017 Aug;92(2):166-171. doi: 10.1111/cge.12948. Epub 2017 Jan 16. Clin Genet. 2017. PMID: 27925162
592 results