Marbach-Rustad progeroid syndrome
MONDO:0859147Mondo
Findings
No curated finding names Marbach-Rustad progeroid syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
32 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.
- Delayed eruption of primary teethHPOHP:0000680
- 2 of 2 reported patients
- Eruption failureHPOHP:0000706
- 2 of 2 reported patients
- Growth delayHPOHP:0001510
- 2 of 2 reported patients
- HypodontiaHPOHP:0000668
- 2 of 2 reported patients
- Intention tremorHPOHP:0002080
- 2 of 2 reported patients
- MicrocephalyHPOHP:0000252
- 2 of 2 reported patients
- Prominent superficial veinsHPOHP:0001015
- 2 of 2 reported patients
- ProptosisHPOHP:0000520
- 2 of 2 reported patients
- Shallow orbitsHPOHP:0000586
- 2 of 2 reported patients
- CNS hypomyelinationHPOHP:0003429
- 1 of 2 reported patients
- Complete right bundle branch blockHPOHP:0011712
- 1 of 2 reported patients
- Convex nasal ridgeHPOHP:0000444
- 1 of 2 reported patients
Show the remaining 20
- Femur fractureHPOHP:0031846
- 1 of 2 reported patients
- Hyperintensity of cerebral white matter on MRIHPOHP:0030890
- 1 of 2 reported patients
- Insulin resistanceHPOHP:0000855
- 1 of 2 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 1 of 2 reported patients · Antenatal onset
- Large foreheadHPOHP:0002003
- 1 of 2 reported patients
- MicrognathiaHPOHP:0000347
- 1 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.
- LEMD2HGNC:21244
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · G2P · Autosomal dominant · 2025
- Limited · Ambry Genetics · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
2 names
Resolves to: Marbach-Rustad progeroid syndrome
- Also called
- LEMD2-associated nuclear envelopathy with early progeroid appearanceWormian bones-micrognathia-abnormal dentition-progeroid syndrome