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1,613 Possible Causes for Cerebellar Hypoplasia, Hydrocephalus

  • Arnold-Chiari Malformation Type 1

    In symptomatic patients, it is associated with: spinal diseases - 50% of cases: syringomyelia hydromyelia cranial disorders - 10% of cases: obstructive hydrocephalus Links[] hypoplasia without displacement of the cerebellum through the foramen magnum probably a variation of cerebellar hypoplasia Chiari V malformation absent cerebellum herniation[] Patients with atlantoaxial instability, tethered cord, associated myelomeningocele, hydrocephalus, or elevated intracranial pressure were excluded.[]

  • Dandy-Walker Syndrome

    An adult with asymptomatic Dandy-Walker malformation without hydrocephalus was studied.[] hypoplasia, hydrocephalus, and posterior fossa cyst formation.[] Optimal treatment for hydrocephalus related to Dandy-Walker syndrome (DWS) remains elusive.[]

  • Aprosencephaly and Cerebellar Dysgenesis

    Hydrocephalus occurs in most cases. Agenesis of corpus callosum, hydrocephalus and occipital meningocele.[] This article is about human cerebellar hypoplasia. For cerebellar hypoplasia in other animals, see cerebellar hypoplasia (non-human).[] hydrocephalus, arthrogryposis hypomyelination - border disease hypomyelination - border disease Anencephaly, Aprosencephaly Anencephaly, Aprosencephaly Hydromyelia-Syringomyelia[]

  • Arnold Chiari Malformation

    Abstract Cortical biopsies of 13 patients with clinical diagnosis of congenital hydrocephalus, Arnold-Chiari malformation and hydrocephalus, and postmeningitis hydrocephalus[] Type IV is a form a cerebellar hypoplasia.[] We report the second case of focal dermal hypoplasia associated with myelomenigocele, Arnold-Chiari malformation and hydrocephalus and the first in a male.[]

  • Craniosynostosis-Dandy-Walker Malformation-Hydrocephalus Syndrome

    , with Dandy-Walker malformation and hydrocephalus.[] Showing of 14 80%-99% of people have these symptoms Cerebellar hypoplasia Small cerebellum Underdeveloped cerebellum [ more ] 0001321 Dandy-Walker malformation 0001305 Dolichocephaly[] Orpha Number: 1538 Disease definition Craniosynostosis , Dandy-Walker malformation and hydrocephalus is a malformation disorder characterized by sagittal craniosynostosis[]

  • Mega-Cisterna Magna

    Two of the three male children have, in addition, congenital communicating hydrocephalus associated with agenesis of the posterior cerebellar vermis.[] Differential diagnosis includes Dandy-Walker malformations and variants , cerebellar hypoplasia, posterior fossa arachnoid cyst , and epidermoid cysts .[] Familial communicating hydrocephalus, posterior cerebellar agenesis, mega cisterna magna, and port-wine nevi. Report on five members of one family.[]

  • TORCH Syndrome

    There was an associated moderate hydrocephalus with cerebral cortical atrophy.[] The MRI scan of the brain showed cerebellar hypoplasia in one of the boys, while the cerebellum had normal size in the other.[] […] such as fever, lethargy, poor feeding, petechiae on the skin, purpura, pneumonia, hepatosplenomegaly, jaundice, hemolytic and other anemias, encephalitis, microcephaly, hydrocephalus[]

  • Lissencephaly

    Progressive hydrocephalus (an excessive accumulation of cerebrospinal fluid in the brain) is very rare, seen only in the subtype of Walker-Warburg syndrome, but may require[] A newborn with a rare type of lissencephaly is reported, characterized by extreme cerebral and cerebellar hypoplasia.[] Hydrocephalus may require treatment with a VP shunt, a tube that goes from the brain through a hole placed in the skull and then under the skin all the way to the abdomen,[]

  • Arnold-Chiari Malformation Type 2

    Signs and symptoms Clinical features of hydrocephalus are influenced by the patient's age, the cause of the hydrocephalus, the location of the obstruction, its duration, and[] Type IV is a form a cerebellar hypoplasia.[] 2015 ICD-9-CM Diagnosis Code 741.0 Spina bifida with hydrocephalus There are 4 ICD-9-CM codes below 741.0 that define this diagnosis in greater detail.[]

  • Cerebellotrigeminal Dermal Dysplasia

    Neuroimaging of patients with GLHS shows rhombencephalosynapsis is universally present, with ventriculomegaly/hydrocephalus and cerebellar hypoplasia being common.[] […] hormone (GH) deficiency was ruled out in all patients, although one of them might have developed secondary GH deficiency due to partial hypopituitarism following severe hydrocephalus[] Poretti A, Limperopoulos C, Roulet-Perez E et al (2010) Outcome of severe unilateral cerebellar hypoplasia.[]

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