Hypoplasia or agenesis of cerebellar hemispheres (Q46035): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Hipoplasia cerebelar corresponde ao subdesenvolvimento de estruturas cerebelares, que pode envolver o vermis e/ou os hemisférios cerebelares de agenesia parcial a total. Tem sido descrita no contexto de várias entidades clínicas: anomalias cromossômicas, exposição intrauterina a toxinas e agentes infecciosos, distúrbios metabólicos (distúrbios de glicosilação e deficiências de CoQ10) e uma grande variedade de doenças neurológicas genéticas raras. Pode estar restrita ao cerebelo ou afetar outras estruturas do SNC: o mesencéfalo (síndromes dentais molares), ponte e medula (hipoplasia ponto-cerebelar), córtex cerebral (síndromes de hipoplasia cerebelar com lissencefalia).
@@ description / en / description / en @@
+Cerebellar hypoplasia corresponds to underdevelopment of cerebellar structures that can involve the vermis and/or the cerebellar hemispheres from partial to total agenesis. It has been described in the context of various clinical entities: chromosomal anomalies, in utero exposure to toxins and infectious agents, metabolic disorders (disorders of glycosylation and CoQ10 deficiencies), and a wide variety of rare genetic neurological diseases. It can be confined to the cerebellum, or affect other CNS structures: the midbrain (molar tooth syndromes), pons and medulla (ponto-cerebellar hypoplasia), cerebral cortex (lissencephaly cerebellar hypoplasia syndromes).
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+CID11:LA06.1
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@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-13T00:00:00Z
-Timezone
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 Before
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@@ Property / Collection date: 13 August 2026 / rank @@
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@@ Property / Linked ICD 10 @@
+Q07.9
@@ Property / Linked ICD 10: Q07.9 / rank @@
+Normal rank

Latest revision as of 14:21, 13 August 2026

Cerebellar hypoplasia corresponds to underdevelopment of cerebellar structures that can involve the vermis and/or the cerebellar hemispheres from partial to total agenesis. It has been described in the context of various clinical entities: chromosomal anomalies, in utero exposure to toxins and infectious agents, metabolic disorders (disorders of glycosylation and CoQ10 deficiencies), and a wide variety of rare genetic neurological diseases. It can be confined to the cerebellum, or affect other CNS structures: the midbrain (molar tooth syndromes), pons and medulla (ponto-cerebellar hypoplasia), cerebral cortex (lissencephaly cerebellar hypoplasia syndromes).

Language	Label	Description	Also known as
default for all languages	LA06.1
English	Hypoplasia or agenesis of cerebellar hemispheres	Cerebellar hypoplasia corresponds to underdevelopment of cerebellar structures that can involve the vermis and/or the cerebellar hemispheres from partial to total agenesis. It has been described in the context of various clinical entities: chromosomal anomalies, in utero exposure to toxins and infectious agents, metabolic disorders (disorders of glycosylation and CoQ10 deficiencies), and a wide variety of rare genetic neurological diseases. It can be confined to the cerebellum, or affect other CNS structures: the midbrain (molar tooth syndromes), pons and medulla (ponto-cerebellar hypoplasia), cerebral cortex (lissencephaly cerebellar hypoplasia syndromes).