[
    {
        "id": "osp-11478",
        "type": "article-journal",
        "title": "Caudal Regression Syndrome with Partial Agenesis of the Corpus callosum and Partial Lobar Holoprosencephaly: Case report",
        "author": [
            {
                "family": "Al Hashami",
                "given": "Hilal"
            },
            {
                "family": "Bataclan",
                "given": "Maria F."
            },
            {
                "family": "Krishnan",
                "given": "Mariam"
            },
            {
                "family": "Lalitha",
                "given": ""
            }
        ],
        "URL": "https://omanscience.com/ar/articles/caudal-regression-syndrome-with-partial-agenesis-of-the-corpus-callosum-and-partial-lobar-holoprosencephaly-case-report",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2025
                ]
            ]
        },
        "container-title": "Sultan Qaboos University Medical Journal",
        "volume": "10",
        "issue": "1",
        "page": "89-93",
        "DOI": "10.18295/2075-0528.1164",
        "publisher": "Sultan Qaboos University",
        "ISSN": "2075-051X",
        "abstract": "Caudal regression syndrome is a rare fetal condition of diabetic pregnancy. Although the exact mechanism is not known, hyperglycaemia during embryogenesis seems to act as a teratogen. Independently, caudal regression syndrome (CRS), agenesis of the corpus callosum (ACC) and partial lobar holoprosencephaly (HPE) have been reported in infants of diabetic mothers. To our knowledge, a combination of all these three conditions has not been reported so far."
    }
]