Pontocerebellar hypoplasia type 2 (Q90404): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Hipoplasia pontocerebelar tipo 2 é o subtipo mais comum de hipoplasia pontocerebelar caracterizada por início neonatal e ausência de desenvolvimento motor voluntário e posterior microencefalia progressiva, clônus generalizado, desenvolvimento de coreia e espasticidade. A maioria dos pacientes não atingirá a puberdade.
@@ description / en / description / en @@
+Pontocerebellar hypoplasia type 2 is the most common subtype of pontocerebellar hypoplasia characterised by neonatal onset and a lack of voluntary motor development and later progressive microencephaly, generalised clonus, development of chorea and spasticity. The majority of patients will not reach puberty.
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+https://id.who.int/icd/entity/1158649247
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+CID11:ID_1158649247
@@ Property / CURIE: CID11:ID_1158649247 / rank @@
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+Concluído
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@@ Property / Knowledge Architect @@
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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
++00:00
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+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest revision as of 17:22, 15 August 2026

Pontocerebellar hypoplasia type 2 is the most common subtype of pontocerebellar hypoplasia characterised by neonatal onset and a lack of voluntary motor development and later progressive microencephaly, generalised clonus, development of chorea and spasticity. The majority of patients will not reach puberty.

Language	Label	Description	Also known as
default for all languages	ID_1158649247
English	Pontocerebellar hypoplasia type 2	Pontocerebellar hypoplasia type 2 is the most common subtype of pontocerebellar hypoplasia characterised by neonatal onset and a lack of voluntary motor development and later progressive microencephaly, generalised clonus, development of chorea and spasticity. The majority of patients will not reach puberty.