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At birth, the presence of collodion membrane was confirmed and subsequently, the diagnosis of an autosomal recessive congenital ichthyosis due to compound heterozygosity of the <jats:italic>TGM1<\/jats:italic> gene was made.<\/jats:p>","DOI":"10.1111\/pde.15506","type":"journal-article","created":{"date-parts":[[2023,12,29]],"date-time":"2023-12-29T12:01:06Z","timestamp":1703851266000},"page":"512-514","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Prenatal ultrasound detection of collodion membrane in association with an autosomal recessive congenital ichthyosis due to transglutaminase 1 deficiency"],"prefix":"10.1111","volume":"41","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2206-8909","authenticated-orcid":false,"given":"Adalgisa","family":"Cordisco","sequence":"first","affiliation":[{"name":"Division of Prenatal Diagnosis Azienda USL Toscana Centro, San Giovanni di Dio Hospital  Firenze 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