Female phenotype at birth and postnatal masculinization, during the first months of life, associated with transient 5α-reductase 2 deficiency in a preterm infant. A timing defect syndrome?

M. Vuerich, P. Ghirri, I. Merusi, A. Cuttano, F. Baldinotti, P. Simi, C. J. Migeon, Antonio Boldrini

Research output: Contribution to journalArticlepeer-review

Original languageEnglish (US)
Pages (from-to)82
Number of pages1
JournalMinerva pediatrica
Issue number5 SUPPL. 1
StatePublished - Oct 2003
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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