Paganini-Miozzo syndrome
MONDO:0026724Mondo
Findings
No curated finding names Paganini-Miozzo syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked recessive inheritance
- Onset and course
- 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.
- Deeply set eyeHPOHP:0000490
- 2 of 2 reported patients
- Delayed ability to walkHPOHP:0031936
- 2 of 2 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Downslanted palpebral fissuresHPOHP:0000494
- 2 of 2 reported patients
- Downturned corners of mouthHPOHP:0002714
- 2 of 2 reported patients
- Febrile seizure (within the age range of 3 months to 6 years)HPOHP:0002373
- 2 of 2 reported patients
- Feeding difficultiesHPOHP:0011968
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- High myopiaHPOHP:0011003
- 2 of 2 reported patients
- HyperalaninemiaHPOHP:0003348
- 2 of 2 reported patients
- Increased circulating lactate concentrationHPOHP:0002151
- 2 of 2 reported patients
- Large foreheadHPOHP:0002003
- 2 of 2 reported patients
Show the remaining 12
- Lateral ventricle dilatationHPOHP:0006956
- 2 of 2 reported patients
- Low-set earsHPOHP:0000369
- 2 of 2 reported patients
- Malar flatteningHPOHP:0000272
- 2 of 2 reported patients
- Mandibular prognathiaHPOHP:0000303
- 2 of 2 reported patients
- MicrotiaHPOHP:0008551
- 2 of 2 reported patients
- Narrow foreheadHPOHP:0000341
- 2 of 2 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.
- HS6ST2HGNC:19133
- Limited · Ambry Genetics · X-linked · 2018
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021
Where it sits
Other names
2 names
Resolves to: Paganini-Miozzo syndrome
- Also called
- mental retardation, X-Linked, syndromic, Paganini-Miozzo typePaganini-Miozzo syndrome, X-linked recessive