Craniosynostosis: before and after successful surgery! #paediatricneurosurgeoninbangladesh #unicoronalcraniosynostosis #anteriorplagiocephaly #craniosynostosis #PaediatricNeuroSurgery #paediatricneurosurgeonindhaka | Neurosurgeon Dr. Md. Ziauddin

Edlord 23 yrs old Crouzon syndrome is a rare genetic disorder. It is a form of craniosynostosis, a condition in which there is premature fusion of the fibrous joints (sutures) between certain bones of the skull. The sutures allow an infant’s head to grow and expand. Eventually, these bones fuse together to form the skull. In Crouzon syndrome, the sutures fuse prematurely affecting the proper growth of the skull and head and potentially altering the shape and development of the skull. Certain bon

Pfeiffer syndrome is a rare genetic disorder characterized by craniosynostosis—premature fusion of the skull bones—present during pregnancy. This condition causes deformities of the head and face, prominent eyes, and short, wide thumbs and toes. This disorder often involves mutations in the FGFR1 or FGFR2 genes. #geneticdisorders #babylove #babycare #nicucare #newbornbaby #babyworld | Yuli Ismalia