Lethal Congenital Contracture Syndrome 10; Lccs10

Description

NEK9-related lethal skeletal dysplasia is a rare, lethal, primary bone dysplasia characterized by fetal akinesia, multiple contractures, shortening of all long bones, short, broad ribs, narrow chest and thorax, pulmonary hypoplasia and a protruding abdomen. Short bowed femurs may also be associated.

Clinical Features

Top most frequent phenotypes and symptoms related to Lethal Congenital Contracture Syndrome 10; Lccs10

  • Micrognathia
  • Flexion contracture
  • High palate
  • Intrauterine growth retardation
  • Short neck
  • Ventricular septal defect
  • Talipes equinovarus
  • Long philtrum
  • Skeletal dysplasia
  • Narrow chest
And another 16 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


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Lethal Congenital Contracture Syndrome 10; Lccs10 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Congenital Contractures Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

FKBP10, COL3A1, FBN1, PLOD3, SLC39A13, PLOD2, ALG2, CHAT, CHRNE, DOK7, NEB, RAPSN, DNM2, LMNA, UBA1, TPM3, ACTA1, CNTN1, TPM2, MYH2 , (...)

View the complete list with 37 more genes
Specificity
2 %
Genes
100 %
Congenital contracture syndrome extended NGS panel.

By Connective Tissue Gene Tests in United States.

DOK7, RAPSN, DNM2, LMNA, TPM2, MUSK, CHRNA1, CHRND, CHRNG, NALCN, FBN2, GLE1, TNNI2, NEK9, TNNT3, MYH3, PIEZO2, GLDN, ADGRG6, ADCY6 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
100 %
Congenital contracture syndrome extended Comprehensive panel.

By Connective Tissue Gene Tests in United States.

DOK7, RAPSN, DNM2, LMNA, TPM2, MUSK, CHRNA1, CHRND, CHRNG, NALCN, FBN2, GLE1, TNNI2, NEK9, TNNT3, MYH3, PIEZO2, GLDN, ADGRG6, ADCY6 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
100 %
Congenital contracture syndrome extended Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

DOK7, RAPSN, DNM2, LMNA, TPM2, MUSK, CHRNA1, CHRND, CHRNG, NALCN, FBN2, GLE1, TNNI2, NEK9, TNNT3, MYH3, PIEZO2, GLDN, ADGRG6, ADCY6 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
100 %
Lethal congenital contracture syndrome and related disorders Comprehensive Panel.

By Connective Tissue Gene Tests in United States.

DOK7, RAPSN, DNM2, LMNA, MUSK, CHRNA1, CHRND, CHRNG, GLE1, NEK9, GLDN, ADGRG6, ADCY6, CNTNAP1, ZBTB42, MYBPC1, ZMPSTE24, PIP5K1C, ERBB3, VPS33B , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
Lethal congenital contracture syndrome and related disorders NGS Panel.

By Connective Tissue Gene Tests in United States.

DOK7, RAPSN, DNM2, LMNA, MUSK, CHRNA1, CHRND, CHRNG, GLE1, NEK9, GLDN, ADGRG6, ADCY6, CNTNAP1, ZBTB42, MYBPC1, ZMPSTE24, PIP5K1C, ERBB3, VPS33B , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
Lethal congenital contracture syndrome and related disorders Deletion / Duplication Panel.

By Connective Tissue Gene Tests in United States.

DOK7, RAPSN, DNM2, LMNA, MUSK, CHRNA1, CHRND, CHRNG, GLE1, NEK9, GLDN, ADGRG6, ADCY6, CNTNAP1, ZBTB42, MYBPC1, ZMPSTE24, PIP5K1C, ERBB3, VPS33B , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
NEK9.

By Fulgent Genetics Fulgent Genetics in United States.

NEK9
Specificity
100 %
Genes
100 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ABCB11, ABCB4, FKBP10, FOXL2, HNF1A, PPARG , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
100 %

Alternate names

Lethal Congenital Contracture Syndrome 10; Lccs10 Is also known as ;lethal skeletal dysplasia-fetal akinesia-contractures-thoracic dysplasia-pulmonary hypoplasia syndrome.


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