Zobrazeno 1 - 2
of 2
pro vyhledávání: '"AbdulAli P. Zada"'
Autor:
Safa Eltahir, Wadha Alotaibi, Khalid Al-Mobaireek, Abdulali P. Zada, Adnan Zafar, Gawahir Mukhtar, Mohammed Alzaid, Mohammed Almannai
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 4, Pp 258-263 (2021)
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics & Adolescent Medicine
Background Primary ciliary dyskinesia (PCD) is a ciliopathy with diverse clinical and genetic findings caused by abnormal motile cilia structure and function. In this study, we describe the clinical characteristics of confirmed PCD cases in our popul
Autor:
Eissa Faqeih, Rasim Ozgur Rosti, Mohammad A. M. Saleh, Laila Bastaki, AbdulAli P. Zada, Joseph G. Gleeson, Kyongmi Um, Emily Spencer
Publikováno v:
American Journal of Medical Genetics Part A. 167:805-809
Microcephaly-capillary malformation syndrome (MIC-CAP syndrome) is a newly recognized autosomal recessive congenital neurocutaneous central nervous system disorder characterized by severe microcephaly, early-onset seizures, profound psychomotor disab