Fazio-londe Disease

Description

Fazio-Londe disease is a progressive bulbar palsy with onset in childhood that presents with hypotonia and respiratory insufficiency (summary by Bosch et al., 2011).

Clinical Features

Top most frequent phenotypes and symptoms related to Fazio-londe Disease

  • Generalized hypotonia
  • Hearing impairment
  • Failure to thrive
  • Sensorineural hearing impairment
  • Muscle weakness
  • Ptosis
  • Hyperreflexia
  • Dysphagia
  • Respiratory insufficiency
  • Facial palsy

And another 15 symptoms. If you need more information about this disease we can help you.

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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

Fazio-londe Disease Is also known as bulbar palsy, progressive, of childhood.

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.

Fazio-londe Disease Recommended genes panels

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

By Genetic Services Laboratory University of Chicago (United States).

BCS1L, RTN2, SACS, SCN1A, SCN2A, SCN8A, SCO1, SDHA, SDHD, SLC16A2, SLC17A5, SLC19A2, SLC1A3, SLC20A2, SLC2A1, SLC6A1, SLC9A1, SLC9A6, SNAP25, SOD1 , (...)

View the complete list with 457 more genes
Specificity
1 %
Genes
100 %
OtoGenome Test for Hearing Loss (110 Genes).

By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine (United States).

BCS1L, SIX1, SNAI2, SMPX, SOX10, TECTA, TIMM8A, TMPRSS3, USH1C, USH2A, CLRN1, WFS1, ESPN, CLIC5, CDH23, CABP2, RIPOR2, CACNA1D, ACTG1, PCDH15 , (...)

View the complete list with 89 more genes
Specificity
1 %
Genes
100 %
Fatty acid metabolism/ketogenesis disorders.

By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust (United Kingdom).

SLC22A5, SLC25A20, SLC52A3, ACAD9, CPT1A, CPT1B, CPT2, SLC52A2, SLC52A1, ETFA, ETFB, ETFDH, HADH, HADHA, HADHB, HMGCL, HMGCS2, ACADM, ACADVL
Specificity
6 %
Genes
100 %
Fatty acid metabolism/ketogenesis disorders.

By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust (United Kingdom).

SLC22A5, SLC25A20, SLC52A3, ACAD9, CPT1A, CPT1B, CPT2, SLC52A2, SLC52A1, ETFA, ETFB, ETFDH, HADH, HADHA, HADHB, HMGCL, HMGCS2, ACADM, ACADVL
Specificity
6 %
Genes
100 %
Audiome (hearing loss panel).

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).

BCS1L, SIX1, SNAI2, SMPX, SOX10, SUCLA2, TECTA, TIMM8A, TMPRSS3, USH1C, USH2A, CLRN1, TSPEAR, WFS1, ESPN, CLIC5, CDH23, CABP2, PCDH15, OSBPL2 , (...)

View the complete list with 85 more genes
Specificity
1 %
Genes
100 %
Brown-Vialetto-Van Laere syndrome 1 (sequence analysis of SLC52A3 gene).

By CGC Genetics (Portugal).

SLC52A3
Specificity
100 %
Genes
100 %
Fazio-Londe disease (sequence analysis of SLC52A3 gene).

By CGC Genetics (Portugal).

SLC52A3
Specificity
100 %
Genes
100 %
Fazio-Londe disease (deletion/duplication analysis of SLC52A3 gene).

By CGC Genetics (Portugal).

SLC52A3
Specificity
100 %
Genes
100 %

You can get up to 25 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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