neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
MONDO:0060759Mondo
Findings
No curated finding names neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset · Juvenile onset · Progressive · Childhood onset
HPO, annotations 2026-09-02
Features
24 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Absent speechHPOHP:0001344
- 5 of 5 reported patients
- Intellectual disabilityHPOHP:0001249
- 7 of 7 reported patients
- SeizureHPOHP:0001250
- 7 of 7 reported patients
- Loss of ambulationHPOHP:0002505
- 6 of 7 reported patients
- Developmental regressionHPOHP:0002376
- 5 of 7 reported patients
- DystoniaHPOHP:0001332
- 4 of 7 reported patients
- Global developmental delayHPOHP:0001263
- 3 of 6 reported patients
- AtaxiaHPOHP:0001251
- 3 of 7 reported patients
- DysphagiaHPOHP:0002015
- 3 of 7 reported patients
- Cerebellar atrophyHPOHP:0001272
- 2 of 7 reported patients
- Cerebral atrophyHPOHP:0002059
- 2 of 7 reported patients
- ChoreoathetosisHPOHP:0001266
- 2 of 7 reported patients
Show the remaining 12
- SpasticityHPOHP:0001257
- 2 of 7 reported patients
- Babinski signHPOHP:0003487
- 1 of 5 reported patients
- HyperreflexiaHPOHP:0001347
- 1 of 5 reported patients
- Positive Romberg signHPOHP:0002403
- 1 of 5 reported patients
- Corpus callosum atrophyHPOHP:0007371
- 1 of 7 reported patients
- EsotropiaHPOHP:0000565
- 1 of 7 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- IRF2BPLHGNC:14282
- Definitive · Ambry Genetics · Autosomal dominant · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · G2P · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2018
Where it sits
Other names
1 name
Resolves to: neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
- Also called
- IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome