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Dandy–Walker malformation (DWM), also known as Dandy–Walker syndrome (DWS), is a rare congenital brain malformation in which the part joining the two hemispheres of the cerebellum (the cerebellar vermis) does not fully form, and the fourth ventricle and space behind the cerebellum (the posterior fossa) are enlarged with cerebrospinal fluid.
Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome (HCDPH1, also known as Sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus, Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus, Braddock-Jones-Superneau syndrome, or simply Hydrocephalus, autosomal dominant) is an autosomal dominant ...
Arthur Earl Walker (March 12, 1907 – January 1, 1995) was a Canadian-born American neurosurgeon, neuroscientist and epileptologist remembered for the eponymous syndromes Dandy–Walker syndrome, Dandy–Walker-like syndrome [1] and Walker–Warburg syndrome. During his career he published over 400 research articles and 8 books. [2]
A sonogram before their birth showed Sinny had a hole in heart and she was diagnosed with Dandy-Walker syndrome, a rare congenital disorder that affects brain development.
Dahlberg Borer Newcomer syndrome; Dandy–Walker syndrome; De Barsy syndrome; de Clérambault's syndrome; De Quervain syndrome; De Winter syndrome; Dead arm syndrome; Deficiency of the interleukin-1–receptor antagonist; Degenerative disc disease; Dejerine–Roussy syndrome; Delayed sleep phase disorder; Delusional misidentification syndrome ...
A variety of brain abnormalities are also associated with 13q deletion. They can include epilepsy, craniosynostosis (premature closing of the skull bones), spastic diplegia, cerebral hypotrophy, underdevelopment or agenesis of the corpus callosum, cerebellar hypoplasia, deafness, and, rarely, hydrocephalus, Dandy–Walker syndrome, and spina ...
Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome: Sagittal Dolichocephaly [66] Craniosynostosis-fibular aplasia syndrome [67] Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome Sagittal Scaphocephaly [68] Craniosynostosis-intellectual disability syndrome of 51N and Gettig [69]
Marden–Walker syndrome (MWS) is a rare autosomal recessive congenital disorder. [ 1 ] [ 2 ] It is characterized by blepharophimosis , microcephaly , micrognathia , multiple joint contractures , arachnodactyly , camptodactyly , kyphoscoliosis and delayed motor development and is often associated with cystic dysplastic kidneys , dextrocardia ...