Neonatal Screening of Biotinidase Deficiency: Genotype-phenotype Correlation and Clinical Follow-up
Neonatal Screening of Biotinidase Deficiency: Genotype-phenotype Correlation and Clinical Follow-up
Recruiting · NCT06723925 · Registry updated 2026-03-12Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Neonatal Screening of Biotinidase Deficiency: Genotype-phenotype Correlation and Clinical Follow-up | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, biotinidase deficiency, hereditary disease, inborn carbohydrate metabolic disorder, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, multiple carboxylase deficiency | Recruiting | Not stated | 2026-03-12 | NCT06723925 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | 331 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | Bologna | Italy | 82 |