JOURNAL ARTICLE

Prenatal ultrasound detection of collodion membrane in association with an autosomal recessive congenital ichthyosis due to transglutaminase 1 deficiency.

  • Published In: Pediatric Dermatology, 2024, v. 41, n. 3. P. 512 1 of 3

  • Database: Academic Search Ultimate 2 of 3

  • Authored By: Cordisco, Adalgisa; Lozza, Virginia; Di Marco, Chiara; Cecconi, Antonella; Pisaneschi, Elisa; Berti, Samantha Federica; Adamo, Laura; Lori, Ilaria; Belli, Gilda; Gambi, Beatrice 3 of 3

Abstract

We describe a case of collodion baby diagnosed prenatally by ultrasound. Classic signs (ectropion, flattened nose, and eclabion) were detected on routine ultrasound at 21 weeks of gestation. 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 TGM1 gene was made. [ABSTRACT FROM AUTHOR]

Additional Information

  • Source:Pediatric Dermatology. 2024/05, Vol. 41, Issue 3, p512
  • Document Type:Article
  • Subject Area:Consumer Health
  • Publication Date:2024
  • ISSN:0736-8046
  • DOI:10.1111/pde.15506
  • Accession Number:177219452
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