Roifman syndrome
Roifman syndrome
Explore linked clinical trials. Standard reference: MONDO:00147222 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Primordial Dwarfism Registry | DNA ligase IV deficiency, Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies, Lowry-Wood syndrome, Meier-Gorlin syndrome, Roifman syndrome, Seckel syndrome 1, microcephalic osteodysplastic dysplasia, Saul-Wilson type, microcephalic osteodysplastic primordial dwarfism type II | Recruiting | Not stated | 2025-10-01 | NCT04569149 | |
| Study of the Pathophysiology of RNU4ATAC and RTTN Associated Syndromes | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lowry-Wood syndrome, Roifman syndrome, hereditary disease, microcephalic osteodysplastic primordial dwarfism type I, microcephalic osteodysplastic primordial dwarfism types I and III | Recruiting | Not applicable | 2024-10-09 | NCT06111950 |