Myasthenic Syndrome, Congenital, 22; Cms22
Clinical Features
Top most frequent phenotypes and symptoms related to Myasthenic Syndrome, Congenital, 22; Cms22
- Intellectual disability
- Short stature
- Generalized hypotonia
- Muscle weakness
- Ptosis
- Feeding difficulties
- Motor delay
- Dysarthria
- Hypogonadism
- Neonatal hypotonia
And another 7 symptoms. If you need more information about this disease we can help you.
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.
Alternative names
Myasthenic Syndrome, Congenital, 22; Cms22 Is also known as prepl deficiency.
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.Myasthenic Syndrome, Congenital, 22; Cms22 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Neuromuscular Disorders Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
RYR1, BIN1, SCN4A, SGCA, SGCB, SGCD, SGCG, SNAP25, STIM1, SYT2, TCAP, TNNT1, TNXB, TPM2, TPM3, MYOT, TTN, VCP, ACTA1, RXYLT1 , (...)
View the complete list with 91 more genes
Specificity
1 %
Genes
100 % |
Congenital Myasthenic Syndrome Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
SCN4A, SNAP25, SYT2, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE, COL13A1, COLQ, ALG2, DOK7, ALG14, DPAGT1, PREPL, AGRN, GFPT1, LRP4, MUSK, RAPSN
Specificity
5 %
Genes
100 % |
Congenital Myasthenic Syndrome Deletion/Duplication Panel.
By Genetic Services Laboratory University of Chicago (United States).
SCN4A, SNAP25, SYT2, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE, COL13A1, COLQ, ALG2, DOK7, ALG14, DPAGT1, PREPL, AGRN, GFPT1, LRP4, MUSK, RAPSN
Specificity
5 %
Genes
100 % |
Mitochondrial Disorders Panel (mtDNA Sequencing, Nuclear Genes Sequencing, and Deletion/Duplication).
By ARUP Laboratories, Molecular Genetics and Genomics (United States).
BCS1L, SCO1, SCO2, SDHB, SDHC, SDHD, SLC22A5, SLC25A13, SLC25A15, SLC25A3, SLC25A4, SLC3A1, SPG7, SUCLA2, SUCLG1, SUOX, SURF1, TAZ, TWNK, TIMM8A , (...)
View the complete list with 130 more genes
Specificity
1 %
Genes
100 % |
Hypotonia-cystinuria syndrome (sequence analysis of PREPL gene).
By CGC Genetics (Portugal).
PREPL
Specificity
100 %
Genes
100 % |
Hypotonia-cystinuria syndrome (deletion/duplication analysis of PREPL, SLC3A1 and SLC7A9 genes).
By CGC Genetics (Portugal).
SLC3A1, SLC7A9, PREPL
Specificity
34 %
Genes
100 % |
Hypotonia-cystinuria syndrome (deletion/duplication analysis of PREPL, SLC3A1 and SLC7A9 genes).
By CGC Genetics (Portugal).
SLC3A1, SLC7A9, PREPL
Specificity
34 %
Genes
100 % |
Comprehensive Neuromuscular Sequencing Panel.
By PreventionGenetics PreventionGenetics (United States).
RYR1, BIN1, SCN4A, SGCA, SGCB, SGCD, SGCG, SNAP25, SQSTM1, STIM1, SYT2, TCAP, TIA1, TNNI2, TNNT1, TNNT3, TPM2, TPM3, MYOT, TTN , (...)
View the complete list with 104 more genes
Specificity
1 %
Genes
100 % |
You can get up to 14 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 MULTIPLE FIBROADENOMAS OF THE BREAST; MFAB CATARACT 3, MULTIPLE TYPES; CTRCT3 ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD FAMILIAL THROMBOCYTOSIS CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S MACULAR DEGENERATION, AGE-RELATED, 2; ARMD2 DEAFNESS, X-LINKED 5; DFNX5