Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delay

Saskia Koene, Leo A.J. Kluijtmans, Ron Wevers, Donald Mock, Marcel Pasch, Eva Morava

Research output: Contribution to journalArticlepeer-review

Original languageEnglish (US)
Pages (from-to)195-198
Number of pages4
JournalClinical Dysmorphology
Issue number3
StatePublished - Jul 2008

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Anatomy
  • Pathology and Forensic Medicine
  • Genetics(clinical)

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