Dursun-Ozgul neurodevelopmental syndrome
MONDO:0979898Mondo
Findings
No curated finding names Dursun-Ozgul 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
- Infantile onset · Juvenile onset · Neonatal onset · Childhood onset
HPO, annotations 2026-09-02
Features
115 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
- 10 of 10 reported patients
- Axial dystoniaHPOHP:0002530
- 1 of 1 reported patient
- Axial hypotoniaHPOHP:0008936
- 3 of 3 reported patients
- Babinski signHPOHP:0003487
- 2 of 2 reported patients
- BrachydactylyHPOHP:0001156
- 1 of 1 reported patient
- Broad chinHPOHP:0011822
- 6 of 6 reported patients
- Coarse facial featuresHPOHP:0000280
- 2 of 2 reported patients
- Deeply set eyeHPOHP:0000490
- 4 of 4 reported patients
- Delayed CNS myelinationHPOHP:0002188
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 4 of 4 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 1 of 1 reported patient
- DroolingHPOHP:0002307
- 1 of 1 reported patient
Show the remaining 103
- DysmetriaHPOHP:0001310
- 2 of 2 reported patients
- DysphagiaHPOHP:0002015
- 1 of 1 reported patient
- EEG with burst suppressionHPOHP:0010851
- 1 of 1 reported patient
- EEG with focal slow activityHPOHP:0010843
- 1 of 1 reported patient
- EMG: positive sharp wavesHPOHP:0030007
- 2 of 2 reported patients
- EpicanthusHPOHP:0000286
- 1 of 1 reported patient