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2,783 Possible Causes for Cerebellar Hypoplasia, Non-Communicating Isolated Syringomyelia, Walking Delay

Did you mean: Cerebellar Hypoplasia, Non-Communicating, Isolated Syringomyelia, Walking Delay

  • Arnold-Chiari Malformation Type 1

    Developmental delays may require further medical follow up for underlying problems.[] hypoplasia without displacement of the cerebellum through the foramen magnum probably a variation of cerebellar hypoplasia Chiari V malformation absent cerebellum herniation[] Type IV is a form a cerebellar hypoplasia.[]

  • Congenital Merosin-Positive Muscular Dystrophy

    Delayed ability to roll over Delayed ability to stand with support Delayed ability to sit alone Delayed ability to walk alone (nearly half walk after 4 years) Mild facial[] The second child, a 3-year-old ambulant girl with subtle learning problems, had mild cerebellar hypoplasia and a large subarachnoid space when scanned at 16 months.[] Some children will walk, but sometimes this can be delayed until the age of five or older. Leg splints are often used to assist a child to walk.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Autosomal Recessive Spastic Paraplegia Type 18

    They all presented in the first 2 years of life with developmental delay, delayed walking, abnormal gait, and mild to severe mental retardation.[] hypoplasia and arthrogryposis 616531 600286 Autosomal recessive PIEZO2 18p11.22-p11.21 ?[] […] motor development Delayed motor skills 0002194 Difficulty walking Difficulty in walking 0002355 Elbow flexion contracture Contractures of elbows Elbow contracture Elbow contractures[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Hoyeraal-Hreidarsson Syndrome

    While most people with dyskeratosis congenita have normal intelligence and development of motor skills such as standing and walking, developmental delay may occur in some[] We report on a boy with prenatal growth retardation, progressive pancytopenia, cerebellar hypoplasia, microcephaly and developmental delay.[] Skin rash Kyphoscoliosis Steppage gait Decreased nerve conduction velocity Progressive muscle weakness Split hand Delayed myelination Juvenile onset Abnormality of the foot[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Joubert Syndrome Type 3

    […] the eyes and thus require regular monitoring. [4] Prognosis [ edit ] In a sample of 19 children, a 1997 study found that 3 died before the age of 3, and 2 never learned to walk[] AB - Cerebellar hypoplasia and slowly progressive ophthalmological symptoms are common features in patients with congenital disorders of glycosylation type I.[] MTS results from hypoplasia of the cerebellar vermis and midbrain-hindbrain malformations.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Dyskeratosis Congenita

    While most people with dyskeratosis congenita have normal intelligence and development of motor skills such as standing and walking, developmental delay may occur in some[] hypoplasia, severe immunodeficiency, enteropathy, and intrauterine growth retardation.[] hypoplasia More severe disorders and complications include The development in 80% of patients, most often in the second decade of life, of bone marrow deficiency of variable[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Dysequilibrium Syndrome

    The recognized symptoms of VLDLRCH are moderate-to-severe intellectual disability, seizures, dysarthria, strabismus and delayed locomotion.[] From Wikipedia, the free encyclopedia Jump to navigation Jump to search VLDLR-associated cerebellar hypoplasia Other names Dysequilibrium syndrome, DES ; Nonprogressive cerebellar[] Children either learn to walk very late (often after age 6 years) or never achieve independent ambulation. Management.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Lissencephaly

    The different areas of development that may be delayed include: Motor skills (Gross and Fine)– e.g. rolling, sitting up, walking or picking up smack objects Speech and language[] A newborn with a rare type of lissencephaly is reported, characterized by extreme cerebral and cerebellar hypoplasia.[] A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema. Neuropediatrics 24, 43–46 ( 1993). 15 DeSilva, U. et al.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Aprosencephaly and Cerebellar Dysgenesis

    Sx include delayed sphincter control and walking, back and leg pain, scoliosis, pes cavus, leg asymmetry. Infants of diabetic mothers are at risk.[] This article is about human cerebellar hypoplasia. For cerebellar hypoplasia in other animals, see cerebellar hypoplasia (non-human).[] hypoplasia.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Craniosynostosis-Dandy-Walker Malformation-Hydrocephalus Syndrome

    […] gross motor development Plagiocephaly Deviation of the 5th finger Inability to walk Open mouth Delayed myelination Poor speech Facial asymmetry Hypoplasia of the corpus callosum[] Showing of 14 80%-99% of people have these symptoms Cerebellar hypoplasia Small cerebellum Underdeveloped cerebellum [ more ] 0001321 Dandy-Walker malformation 0001305 Dolichocephaly[] These symptoms may include: Developmental delays in motor and language skills such as sitting up, walking, and talking Poor muscle tone, balance, and coordination Problems[]

    Missing: Non-Communicating Isolated Syringomyelia

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