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  3. GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15

Glycosylphosphatidylinositol Biosynthesis Defect 15; Gpibd15

Table of contents:

Description

GPIBD15 is an autosomal recessive disorder characterized by delayed psychomotor development, variable intellectual disability, hypotonia, early-onset seizures in most patients, and cerebellar atrophy, resulting in cerebellar signs including gait ataxia and dysarthria. The disorder is caused by a defect in glycosylphosphatidylinositol (GPI) biosynthesis (summary by Nguyen et al., 2017).For a discussion of genetic heterogeneity of GPI biosynthesis defects, see GPIBD1 (OMIM ).

Genes related to Glycosylphosphatidylinositol Biosynthesis Defect 15; Gpibd15

  • GPAA1

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Glycosylphosphatidylinositol Biosynthesis Defect 15; Gpibd15

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Ataxia
  • Hypertelorism
  • Nystagmus
  • Abnormal facial shape
  • Spasticity
  • Cognitive impairment

And another 29 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

Glycosylphosphatidylinositol Biosynthesis Defect 15; Gpibd15 Is also known as developmental delay, epilepsy, cerebellar atrophy, and osteopenia.

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.

Glycosylphosphatidylinositol Biosynthesis Defect 15; Gpibd15 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
GPAA1.

By Fulgent Genetics Fulgent Genetics (United States).

GPAA1
Specificity
100 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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