Lipoyltransferase 1 Deficiency; Lipt1d

Clinical Features

Top most frequent phenotypes and symptoms related to Lipoyltransferase 1 Deficiency; Lipt1d

  • Global developmental delay
  • Generalized hypotonia
  • Hypertension
  • Cerebellar atrophy
  • Hypertonia
  • Coma
  • Dystonia
  • Cerebral cortical atrophy
  • Acidosis
  • Elevated hepatic transaminase
And another 22 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.


Mendelian

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Lipoyltransferase 1 Deficiency; Lipt1d Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Dystonia Exome Panel.

By Genetic Services Laboratory University of Chicago in United States.

AARS2, UQCRQ, ATP7B, AUH, BCS1L, PSEN1, GLB1, HPRT1, POLG, NDUFS4, AFG3L2, FOXRED1, NDUFAF2, PANK2, MECP2, NDUFA12, NDUFA9, TTC19, NDUFA10, SCP2 , (...)

View the complete list with 150 more genes
Specificity
1 %
Genes
100 %
Leigh and Leigh-Like Syndrome Sequencing Panel (Nuclear Genes Only) with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

UQCRQ, BCS1L, C12orf65, DLD, POLG, NDUFS4, FOXRED1, NDUFAF2, COQ9, PDSS2, NDUFA12, LIAS, NDUFA9, PDHB, TTC19, NDUFA10, NUBPL, SUCLA2, TSFM, GFM1 , (...)

View the complete list with 43 more genes
Specificity
2 %
Genes
100 %
Mitochondrial Oxidative Phosphorylation Deficiency Sequencing Panel (Nuclear Genes Only) with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

AARS2, ACAD9, YARS2, UQCRQ, UQCRB, ATP5F1E, ATPAF2, BCS1L, TWNK, C12orf65, ELAC2, OPA1, TRMU, DLD, POLG, NDUFS4, SLC25A4, GARS, AFG3L2, FOXRED1 , (...)

View the complete list with 154 more genes
Specificity
1 %
Genes
100 %
LIPT1.

By Fulgent Genetics Fulgent Genetics in United States.

LIPT1
Specificity
100 %
Genes
100 %
Comprehensive Metabolism Panel.

By Blueprint Genetics in Finland.

HFE, MTHFR, MCCC1, MCCC2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2, ARG1, HLCS, BTD, ATP7B , (...)

View the complete list with 414 more genes
Specificity
1 %
Genes
100 %
Nonketotic Hyperglycinemia / Glycine Encephalopathy Panel.

By Blueprint Genetics in Finland.

LIAS, BOLA3, NFU1, GCSH, GLDC, AMT, GLRX5, LIPT1, SLC6A9
Specificity
12 %
Genes
100 %
LEIGH SYNDROME: NGS PANEL-2.

By Laboratorio de Genetica Clinica SL in Spain.

ACAD9, BCS1L, DLD, NDUFS4, FOXRED1, NDUFAF2, PDSS2, NDUFA12, NDUFA9, PDHB, NDUFAF1, TTC19, NDUFA10, SUCLA2, TUFM, COQ2, SCO2, PDHA1, NDUFA2, COX15 , (...)

View the complete list with 23 more genes
Specificity
3 %
Genes
100 %

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PANCREATIC LIPASE DEFICIENCY; PNLIPD IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1; ICF1 ADAMS-OLIVER SYNDROME 2; AOS2 MARINESCO-SJOGREN SYNDROME; MSS MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 2; CAMRQ2