Focal dermal hypoplasia: The conflicting characteristics of prenatal and long-term follow-up images of skin anomalies.

focal derma hypoplasia long‐term follow up magnetic resonance imaging prenatal diagnosis

Journal

Journal of clinical ultrasound : JCU
ISSN: 1097-0096
Titre abrégé: J Clin Ultrasound
Pays: United States
ID NLM: 0401663

Informations de publication

Date de publication:
27 Aug 2024
Historique:
revised: 07 07 2024
received: 11 06 2024
accepted: 04 08 2024
medline: 27 8 2024
pubmed: 27 8 2024
entrez: 27 8 2024
Statut: aheadofprint

Résumé

To the best of our knowledge, this case presents the first prenatal magnetic resonance imaging diagnosis of focal dermal hypoplasia with long-term follow-up, with important discordance between the prenatal and postnatal imaging characteristics of the skin malformation.

Identifiants

pubmed: 39189300
doi: 10.1002/jcu.23799
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 Wiley Periodicals LLC.

Références

Botting RA, Haniffa M. The developing immune network in human prenatal skin. Immunology. 2020;160(2):149‐156.
Wang Y, Song Z, Zhang L, et al. Genetic analysis and prenatal diagnosis of recessive dystrophic epidermolysis bullosa caused by compound heterozygous variants of the COL7A1 gene in a Chinese family. Front Pediatr. 2022;10:941201.
Fassihi H, Eady RA, Mellerio JE, et al. Prenatal diagnosis for severe inherited skin disorders: 25 years' experience. Br J Dermatol. 2006;154(1):106‐113.
Liu F, Chen X, Tu R, Liu S. Prenatal diagnosis of aplasia cutis congenita of the trunk. Int J Dermatol. 2014;53(10):1269‐1271.
Jelin AC, Glenn OA, Strachowski L, Vargas JE. Membranous aplasia cutis congenita. J Ultrasound Med. 2009;28(10):1393‐1396.
Goltz RW, Peterson WC, Gorlin RJ, Ravits HG. Focal dermal hypoplasia. Arch Dermatol. 1962;86:708‐717.
Mansouri M, Bouzid FZ, Amal S, Hocar O, Aboussair N. Focal dermal hypoplasia: case series. Indian J Dermatol. 2023;68(1):122.
Tenkir A, Teshome S. Goltz syndrome (focal dermal hypoplasia) with unilateral ocular, cutaneous and skeletal features: case report. BMC Ophthalmol. 2010;10:28.

Auteurs

Pedro Teixeira Castro (PT)

Department of Fetal Medicine, Biodesign Laboratory DASA/PUC, Rio de Janeiro, RJ, Brazil.

Ana Paula Pinho Matos (APP)

Department of Fetal Medicine, Biodesign Laboratory DASA/PUC, Rio de Janeiro, RJ, Brazil.

Pedro Daltro (P)

Department of Fetal Medicine, Biodesign Laboratory DASA/PUC, Rio de Janeiro, RJ, Brazil.

Tatiana Fazecas (T)

Department of Fetal Medicine, Biodesign Laboratory DASA/PUC, Rio de Janeiro, RJ, Brazil.

Edward Araujo Júnior (E)

Department of Obstetrics, Paulista School of Medicine - Federal University of São Paulo (EPM-UNIFESP), São Paulo, SP, Brazil.
Discipline of Woman Health, Municipal University of São Caetano do Sul (USCS), São Caetano do Sul, SP, Brazil.

Heron Werner (H)

Department of Fetal Medicine, Biodesign Laboratory DASA/PUC, Rio de Janeiro, RJ, Brazil.

Classifications MeSH