Neonatal Death Caused by Interrupted Aortic Arch Associated With 22q11.2 Deletion Syndrome: An Autopsy Case Report.

Shinkawa, Norihiro; Yamaguchi, Masatoshi; Ozaki, Mamoru; Yukawa, Nobuhiro

Shinkawa, Norihiro; Yamaguchi, Masatoshi; Ozaki, Mamoru; Yukawa, Nobuhiro.

Affiliation

Shinkawa N; From the *Section of Legal Medicine, Department of Social Medicine, Faculty of Medicine, University of Miyazaki; and Radiology Division and Division of Clinical Genetics, Faculty of Medicine, University of Miyazaki Hospital, Miyazaki; and §Division of Genomic Medicine, Kanazawa Medical University, Ishikawa, Japan.

Am J Forensic Med Pathol ; 40(2): 178-182, 2019 Jun.

Article in En | MEDLINE | ID: mdl-30562178

Subject(s)

Aorta, Thoracic/abnormalities; Chromosome Deletion; Chromosomes, Human, Pair 22; Fatal Outcome; Female; Heart Defects, Congenital/genetics; Heart Defects, Congenital/pathology; Humans; Infant, Newborn; Thymus Gland/abnormalities

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aorta, Thoracic / Chromosomes, Human, Pair 22 / Chromosome Deletion Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Newborn Language: En Journal: Am J Forensic Med Pathol Year: 2019 Type: Article Affiliation country: Japan

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