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  1. Mohd Jamil AA, Chua WC, Valayudham VR, Hassan HA, Jalal HA
    Radiol Case Rep, 2024 Jan;19(1):374-377.
    PMID: 38033668 DOI: 10.1016/j.radcr.2023.10.036
    We report a case of acalvaria diagnosed prenatally via ultrasound and MRI. Acalvaria is a rare, fatal congenital condition characterized by the absence of flat bones of the cranial vault, dura mater, and its associated muscles with an intact central nervous system. A 41-year-old gravida 5, para 2 + 2A, presented to us at 26 weeks gestation age (GA) with ultrasound findings of a fragile and hypomineralized skull in the fetus. The patient was not keen on whole-axon sequencing. Fetus magnetic resonance imaging (MRI) revealed large cutaneous/skull nonvisualization of the fetus skull, possibly acrania without anencephaly. She delivered via cesarean section at 37 weeks because of two previous cesarean sections. A female infant weighing 2650 g was born with an intact sac to minimize excessive external pressure to the brain tissue. A diagnosis of acalvaria with bilateral lateral cleft lip and palate was made postdelivery. The infant was managed conservatively per multidisciplinary discussion and expired 3 weeks later.
  2. Jamil AAM, Chua WC, Valayudham VR, Hassan HA, Jalal HA
    Radiol Case Rep, 2024 Mar;19(3):1232.
    PMID: 38259716 DOI: 10.1016/j.radcr.2023.11.061
    [This corrects the article DOI: 10.1016/j.radcr.2023.10.036.].
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