Disease #03407 (LKDMN (Leukoencephalopathy with dystonia and motor neuropathy), OMIM:613724)

Official abbreviation LKDMN
Name Leukoencephalopathy with dystonia and motor neuropathy
OMIM ID 613724
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene SCP2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00089120 patient PubMed: Ardisonne 2015, PubMed: Legati 2016 Severe hypotonia and psychomotor regression with leukoencephalopathy F yes Pakistan Pakistani - - - - LKDMN see paper; ..., severe hypotonia, psychomotor regression, leukoencephalopathy SDHA, SDHAF1, SDHAF2, SDHB, SDHC, SDHD SDHB 1 1 Jean-Pierre Bayley
00398753 721 PubMed: Ferese 2021 2-generation family, 1 affected M - Italy - >59y - - - CMS8, LKDMN Peripheral neuropathy (HP:0009830), Decreased nerve conduction velocity (HP:0000762), Bradyphrenia (HP:0031843), Cognitive impairment (HP:0100543), Paresthesia (HP:0003401) AGRN, SCP2 AGRN, SCP2 2 1 Yvet den Hartog
00435044 Pat1 PMID: 27604842 Leukoencephalopathy due to Complex II Deficiency F yes Lebanon - 02y - - - LKDMN - SDHB SDHB 1 1 Jean-Pierre Bayley
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