Aller au contenu

Call for cases of Heterotopic Tissues in placenta

During the last Annual Meeting of the PPS held in Madrid this year, one of the oral presentations was about heterotopic liver tissue in the placenta. The published literature is poor and it became clear during the discussion that several colleagues had seen similar cases but not published them. Not only liver tissue heterotopia is found in the placenta, but also cortical adrenal tissue, adipose tissue and even a case… Lire la suite »Call for cases of Heterotopic Tissues in placenta

Phenotypic characterization of a WBP11-related pseudo-VATER syndome

Targeted gene/phenotype/disorder under study:WBP11 (OMIM # 619227) AbstractWBP11 (WW domain binding protein 11) plays a critical role in mRNA processing and the Notch signaling pathway. Loss-of-function WBP11 variants have previously been associated with VATER association (PMID: 33276377).We have identified a family with dominantly inherited deleterious WBP11 variation. Clinical features include complex segmentation defects, kidney hypoplasia, and prenatal cerebellar stroke.We aim to characterize the phenotypic spectrum of this dominant VATER association… Lire la suite »Phenotypic characterization of a WBP11-related pseudo-VATER syndome

Journée du 08 DECEMBRE 2023 : “BEST OF” meeting

Dr PETITPAS Charlène : Bartsocas papas syndrome : a case report, French Polynesia Dr LIBBRECHT Sasha : Early second trimester growth restriction, Belgium Dr BREHIN Anne-Claire : Severe Neurologic Phenotypes of a metabolic disorder, France Dr DAP Matthieu : A prenatal case of bilateral microphthalmia, France Dr TESSIER Aude : Bi‑allelic variations in CRB2 lead to non‑communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla, Belgium Dr PISAN… Lire la suite »Journée du 08 DECEMBRE 2023 : “BEST OF” meeting