Disease #01757 (DMC (Dyggve-Melchior-Clausen disease), OMIM:223800)

Official abbreviation DMC
Name Dyggve-Melchior-Clausen disease
OMIM ID 223800
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 DYM
Associated tissues -
Disease features height below 2SD, OFC below 3rd percentile, coarse facies, short neck, short trunk, brachydactyly, barrel chest/pectus carinatum, abdominal distension, lumbar lordosis, restricted major joint mobility, waddling gait, intellectual disability/global developmental delay, no odontoid hypoplasia, platyspondyly, double hump vertebral bodies, short and broad ilia with basilar hypoplasia, lacy iliac crests, rhizomelic upper/lower limbs, irregularities epiphyses, irregularities metaphysis, shortened metacarpals, shortened phalanges, carpal bone irregularities, genua valga
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-01-31 21:02:09 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00359404 Pat56 PubMed: Silveira 2021, Journal: Silveira 2021 - M yes Brazil - - - - - DMC - - DYM 1 1 Maria Dora Jazmin Lacarrubba-Flores
00412708 - - - - yes (Pakistan) - - - - - DMC - DYM DYM 1 1 Asmat Ullah
00423220 family PubMed: Abdullah 2020 5-generation family, 8 affected (5F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - DMC see paperp; ..., skeletal dysplasia, mental retardation, progressive spondyloepimetaphyseal dysplasia, disproportionate short stature, generalized platyspondyly, lacy iliac crest DYM DYM 1 9 Johan den Dunnen
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