Lethal Congenital Contracture Syndrome 4; Lccs4
Genes related to Lethal Congenital Contracture Syndrome 4; Lccs4
- MYBPC1
Clinical Features
Phenotypes and symptoms related to Lethal Congenital Contracture Syndrome 4; Lccs4
- Skeletal muscle atrophy
- Distal arthrogryposis
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Lethal Congenital Contracture Syndrome 4; Lccs4 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
Congenital Contractures Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
SKI, SLC18A3, TNNI2, TNNT3, TPM2, TPM3, UBA1, ZMPSTE24, ACTA1, ADGRG6, SLC5A7, KLHL41, FKBP10, NEK9, NALCN, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE , (...)
View the complete list with 37 more genes
Specificity
2 %
Genes
100 % |
Distal Arthrogryposis Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
TNNI2, TNNT3, TPM2, NALCN, CHST14, PIEZO2, ECEL1, FBN2, MYBPC1, MYH3, MYH8
Specificity
10 %
Genes
100 % |
Distal Arthrogryposis Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
TNNI2, TNNT3, TPM2, NALCN, CHST14, PIEZO2, ECEL1, FBN2, MYBPC1, MYH3, MYH8
Specificity
10 %
Genes
100 % |
Arthrogryposis, distal type 1B (sequence analysis of MYBPC1 gene).
By CGC Genetics (Portugal).
MYBPC1
Specificity
100 %
Genes
100 % |
Distal Arthrogryposis Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
TNNI2, TNNT3, TPM2, NALCN, CHST14, PIEZO2, ECEL1, FBN2, MYBPC1, MYH3, MYH8
Specificity
10 %
Genes
100 % |
Distal Arthrogryposis 1B via MYBPC1 Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
MYBPC1
Specificity
100 %
Genes
100 % |
Congenital contracture syndrome extended NGS panel.
By Connective Tissue Gene Tests (United States).
TNNI2, TNNT3, TPM2, VPS33B, ZMPSTE24, ADGRG6, NEK9, LGI4, NALCN, CHRNA1, CHRND, CHRNG, VIPAS39, ADCY6, PIEZO2, DOK7, GLDN, DNM2, ECEL1, ZBTB42 , (...)
View the complete list with 11 more genes
Specificity
4 %
Genes
100 % |
Congenital contracture syndrome extended Comprehensive panel.
By Connective Tissue Gene Tests (United States).
TNNI2, TNNT3, TPM2, VPS33B, ZMPSTE24, ADGRG6, NEK9, LGI4, NALCN, CHRNA1, CHRND, CHRNG, VIPAS39, ADCY6, PIEZO2, DOK7, GLDN, DNM2, ECEL1, ZBTB42 , (...)
View the complete list with 11 more genes
Specificity
4 %
Genes
100 % |
You can get up to 26 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2 MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES; MSSP GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6; DKCB6 MECKEL SYNDROME 13; MKS13 HYPERINSULINISM DUE TO UCP2 DEFICIENCY
Congenital Contractures Panel.
Arthrogryposis, distal type 1B (sequence analysis of MYBPC1 gene).