cerebellar hypoplasia oor Spaans

cerebellar hypoplasia

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hipoplasia cerebelosa

en
rare disorder in which the cerebellum is either missing entirely or is smaller than usual
es
trastorno neurológico que consiste en un subdesarrollo del cerebelo
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There is no treatment for cerebellar hypoplasia caused by such in utero viral infection.
Atronaría nuestros oídos si lo hicieraLiterature Literature
One form of a pure congenital cerebellar hypoplasia has been mapped to a gene locus on chromosome Xq.
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The currently recognized features of HHS are cerebellar hypoplasia, immunodeficiency, progressive bone marrow failure, and intrauterine growth retardation.
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Unilateral cerebellar hypoplasia is not associated with genetic disorders (Ramaekers et al, 1997).
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Patients with HHS typically present in early childhood with cerebellar hypoplasia, immunodeficiency, progressive bone marrow failure, and intrauterine growth retardation.
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A similar condition known as cerebellar hypoplasia occurs when Purkinje cells fail to develop in utero or die off before birth.
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In contrast to these findings, the results of the national risk evaluation as laid down in the supporting documentation to the notification from Brazil are: Trichlorfon has genotoxic, immunotoxic, teratogenic, and neurotoxic characteristics, causes cerebellar hypoplasia, adverse effects on reproduction and on the hormonal system (endocrine deregulation).
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In the calf, some may be inherited (cerebellar abiotrophy, ataxia, hypoplasia, aplasia etc).
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Anomalies include posterior fossa malformations, including Dandy-Walker complex, cerebellar hypoplasia, atrophy, and dysgenesis/agenesis of the vermis.
En combinación con #-fluorouracilo en bolo/ácido folínico (#-FU/FA) durante un total de # semanas de cada ciclo de # semanas (régimen de Roswell Park). AVF#gParaCrawl Corpus ParaCrawl Corpus
Type IV is a form a cerebellar hypoplasia.
La definición de la categoría de productos y los criterios ecológicos específicos aplicables a la misma serán válidos hasta el # de agosto deParaCrawl Corpus ParaCrawl Corpus
Type IV involves an incomplete or underdeveloped cerebellum—a condition known as cerebellar hypoplasia.
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Much of this research focuses on finding better ways to prevent, treat, and ultimately cure disorders that feature cerebellar hypoplasia.
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It is believed that the cerebellar hypoplasia is due to a defect in the neuronal proliferation and neuronal migration during development of the embryonic nervous system.
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We have already mentioned grade I and II while grades III and IV include an important cerebellar hypoplasia, which has a more negative effect on the malformation.
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The clinical signs associated with a natural KRV infection include foetal resorption in dams, runtin, ataxia, cerebellar hypoplasia and jaundice in suckling rats, and sudden death, scrotal cyanosis, abdominal swelling and dehydration in juvenile rats.
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Cerebellar Vermis Hypoplasia: Causes & Reasons - Symptoma®
que contiene las observaciones que forman parte integrante de la Decisión sobre la aprobación de la gestión en la ejecucióndel presupuesto de la Escuela Europea de Policía para el ejercicioParaCrawl Corpus ParaCrawl Corpus
Congenital infections can affect multiple organ systems, and many are associated with specific brain damage, including microcephaly, calcifications (predominantly periventricular, but also in the basal ganglia and in cerebral parenchyma), ventriculomegaly, neuronal migration disorders (pachygyria, polymicrogyria, lissencephaly, and schizenchephaly), cerebellar hypoplasia, and white matter anomalies (8).
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It may occur with a variety of congenital syndromes, metabolic disorders and neurodegenerative disorders; therefore signs and symptoms may depend upon the associated condition an affected individual has.[1] The most common findings are developmental and speech delay, poor muscle tone (hypotonia), ataxia and abnormal ocular (eye) movements. Cerebellar hypoplasia may range from mild or partial underdevelopment to complete absence (agenesis). It may affect only the cerebellum, or also affect other central nervous system structures.
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Dandy-Walker’s malformation has been classically described through the triad including cystic dilation of the fourth ventricle, hypoplasia of the cerebellar vermis and hydrocephalus.
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Descended cerebellar tonsils with a neurospinal malformation that tethers the spinal cord to the or hypoplasia associated with tentorium aplasia.
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