Hereditary sensory and autonomic neuropathy type II (Q84104): Difference between revisions
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Neuropatia hereditária sensitiva e autonômica tipo 2 (NHSA2) é um transtorno autossômico recessivo caracterizado por perda sensitiva profunda e universal envolvendo fibras nervosas grossas e finas, hipotonia acentuada, fraturas indolores, alterações tróficas, pupilas tônicas, constipação, episódios de apneia. | |||
| description / en | description / en | ||
Hereditary sensory and autonomic neuropathy, type 2 (HSAN2) is an autosomal recessive disorder characterised by profound and universal sensory loss involving large and small fibre nerves, marked hypotonia, painless fractures, trophic changes, tonic pupils, constipation, apnoeic spells. | |||
Revision as of 09:28, 15 August 2026
Hereditary sensory and autonomic neuropathy, type 2 (HSAN2) is an autosomal recessive disorder characterised by profound and universal sensory loss involving large and small fibre nerves, marked hypotonia, painless fractures, trophic changes, tonic pupils, constipation, apnoeic spells.
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| default for all languages | ID_2016844157 |
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| English | Hereditary sensory and autonomic neuropathy type II |
Hereditary sensory and autonomic neuropathy, type 2 (HSAN2) is an autosomal recessive disorder characterised by profound and universal sensory loss involving large and small fibre nerves, marked hypotonia, painless fractures, trophic changes, tonic pupils, constipation, apnoeic spells. |
