Disease #06988 (SMALED (atrophy, muscular, spinal, lower extremity predominant))

Official abbreviation SMALED
Name atrophy, muscular, spinal, lower extremity predominant
OMIM ID -
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2022-12-22 17:16:49 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00428160 patient PubMed: Oliwa 2022 2-generation family, 1 affected, unaffected non carrier parents F - United Kingdom (Great Britain) - 00y11m - - - SMALED see paper; ..., 11m-died; antenatal arthrogryposis, postnatal hypotonia, generalized and respiratory weakness, joint deformities particularly affecting lower limbs, poor swallow; 5m-cataracts, ERG abnormal, visual evoked potentials, global developmental impairments - BICD2 1 1 Johan den Dunnen
00432486 209605 - - M no Germany - - - - - SMALED Talipes equinovarus, Motor delay, Lower limb muscle weakness, Skeletal muscle hyperechogenicity DYNC1H1 DYNC1H1 1 1 Andreas Laner
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