Dworschak-Punetha neurodevelopmental syndrome
MONDO:0859260Mondo
Findings
No curated finding names Dworschak-Punetha neurodevelopmental syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Neonatal onset · Childhood onset
HPO, annotations 2026-09-02
Features
23 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.
- Global developmental delayHPOHP:0001263
- 6 of 7 reported patients
- Autistic behaviorHPOHP:0000729
- 3 of 7 reported patients
- PtosisHPOHP:0000508
- 2 of 7 reported patients
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 7 reported patients
- ColpocephalyHPOHP:0030048
- 1 of 7 reported patients
- Cupped earHPOHP:0000378
- 1 of 7 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 1 of 7 reported patients
- Dilation of Virchow-Robin spacesHPOHP:0012520
- 1 of 7 reported patients
- Dysplastic corpus callosumHPOHP:0006989
- 1 of 7 reported patients
- Elevated circulating creatine kinase activityHPOHP:0003236
- 1 of 7 reported patients
- Large earlobeHPOHP:0009748
- 1 of 7 reported patients
- Lower limb hyperreflexiaHPOHP:0002395
- 1 of 7 reported patients
Show the remaining 11
- MicrocephalyHPOHP:0000252
- 1 of 7 reported patients
- MicrodontiaHPOHP:0000691
- 1 of 7 reported patients
- NystagmusHPOHP:0000639
- 1 of 7 reported patients
- Optic disc hypoplasiaHPOHP:0007766
- 1 of 7 reported patients
- Peripheral axonal neuropathyHPOHP:0003477
- 1 of 7 reported patients
- SeizureHPOHP:0001250
- 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.
- PLXNA1HGNC:9099
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2021
- Limited · G2P · Autosomal recessive · 2025