ASXL1-related Bohring-Optiz Syndrome complicated by Persistent Neonatal Pulmonary Hypertension and Abnormal Alveoli Formation.

ASXL1 Bohring-Opitz syndrome persistent pulmonary hypertension of the newborn respiratory distress syndrome

Journal

European journal of medical genetics
ISSN: 1878-0849
Titre abrégé: Eur J Med Genet
Pays: Netherlands
ID NLM: 101247089

Informations de publication

Date de publication:
16 Oct 2024
Historique:
received: 22 07 2024
revised: 27 09 2024
accepted: 13 10 2024
medline: 19 10 2024
pubmed: 19 10 2024
entrez: 18 10 2024
Statut: aheadofprint

Résumé

Bohring-Opitz syndrome (BOS) is a rare disease with a characteristic facial appearance and limb position. This report describes a case of BOS complicated by persistent pulmonary hypertension of the newborn (PPHN) and formation of abnormal alveoli that was confirmed by autopsy. A female neonate was born by cesarean section at 37 weeks and 2 days of gestation and found to have a nevus flammeus, exophthalmos, abnormal palate, retraction of the mandible, and a posture characteristic of BOS. The patients had severe PPHN requiring inhalation of nitric oxide. Genetic testing revealed a de novo frameshift variant in ASXL1. Autopsy revealed that the lung was at the saccular stage, equivalent to 28-34 weeks of gestation. This is the first report to present pathological evidence of immaturity of the lung that may be associated with PPHN in a patient with BOS caused by a variant in ASXL1.

Identifiants

pubmed: 39423952
pii: S1769-7212(24)00070-3
doi: 10.1016/j.ejmg.2024.104978
pii:
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104978

Informations de copyright

Copyright © 2024. Published by Elsevier Masson SAS.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflict of interests.

Auteurs

Makoto Arioka (M)

Maternal and Perinatal Center, Kagawa University Hospital, Kagawa, Japan. Electronic address: arioka.makoto@kagawa-u.ac.jp.

Shinji Nakamura (S)

Department of Pediatrics, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: nakamura.shinji@kagawa-u.ac.jp.

Katsufumi Nishioka (K)

Department of Pediatrics, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: nishioka.katsufumi@kagawa-u.ac.jp.

Kota Inoue (K)

Department of Pediatrics, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: inoue.kota@kagawa-u.ac.jp.

Yasuhiro Nakao (Y)

Department of Pediatrics, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: nakao.yasuhiro@kagawa-u.ac.jp.

Yumi Miyai (Y)

Department of Pathology and Host Defense, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: miyai.yumi@kagawa-u.ac.jp.

Hirosuke Morita (H)

Maternal and Perinatal Center, Kagawa University Hospital, Kagawa, Japan. Electronic address: morita.hirosuke@kagawa-u.ac.jp.

Kosuke Koyano (K)

Maternal and Perinatal Center, Kagawa University Hospital, Kagawa, Japan. Electronic address: koyano.kosuke@kagawa-u.ac.jp.

Toshiki Takenouchi (T)

Department of Pediatrics, School of Medicine, Keio University, Tokyo, Japan. Electronic address: toshiki.take@keio.jp.

Saneyuki Yasuda (S)

Clinical training center, Kagawa University Hospital, Kagawa, Japan. Electronic address: yasuda.saneyuki@kagawa-u.ac.jp.

Yoichi Chiba (Y)

Department of Pathology and Host Defense, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: chiba.yoichi@kagawa-u.ac.jp.

Takashi Iwase (T)

Department of Pediatrics, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: iwase.takashi@kagawa-u.ac.jp.

Masaki Ueno (M)

Department of Pathology and Host Defense, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: ueno.masaki@kagawa-u.ac.jp.

Takashi Kusaka (T)

Department of Pediatrics, Faculty of Medicine, Kagawa University, Kagawa, Japan. Electronic address: kusaka.takashi@kagawa-u.ac.jp.

Classifications MeSH