3-METHYLCROTONYL COA CARBOXYLASE 2 DEFICIENCY

Clinical trials for 3-METHYLCROTONYL COA CARBOXYLASE 2 DEFICIENCY explained in plain language.

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Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Matched conditions: 3-METHYLCROTONYL COA CARBOXYLASE 2 DEFICIENCY

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 02, 2026 01:00 UTC

3-METHYLCROTONYL COA CARBOXYLASE 2 DEFICIENCY

Get alerted when new 3-METHYLCROTONYL COA CARBOXYLASE 2 DEFICIENCY trials appear

Newborn screening study aims to catch rare diseases at birth