Donarska Julia, Szablewska Anna Weronika, Wierzba Jolanta
Department of Obstetric and Gynaecological Nursing, Institute of Nursing and Midwifery, Medical University of Gdansk, Sklodowskiej-Curie 3A, 80-210 Gdansk, Poland.
Department of Internal and Pediatric Nursing, Institute of Nursing and Midwifery, Medical University of Gdańsk Sklodowskiej-Curie 3A, 80-210 Gdansk, Poland.
J Clin Med. 2025 Feb 9;14(4):1102. doi: 10.3390/jcm14041102.
Maternal phenylketonuria (PKU), a metabolic disorder caused by defective phenylalanine hydroxylase activity, requires strict lifelong dietary management to prevent toxic phenylalanine accumulation. During pregnancy, non-adherence to a low-phenylalanine diet can lead to maternal PKU syndrome, resulting in severe neonatal complications, including microcephaly, congenital heart defects, and growth restrictions. Despite advances in metabolic management and preconception care guidelines, adherence remains a significant challenge, particularly among adults transitioning out of pediatric care. This case report examines the clinical consequences of dietary non-adherence in maternal PKU, highlighting the importance of preconception education, metabolic monitoring, and multidisciplinary care in preventing adverse neonatal outcomes. Using the CARE guidelines, we present the clinical course of a male neonate born to a mother with untreated PKU. The analysis incorporates maternal dietary history, prenatal care details, and neonatal outcomes. Additionally, a review of current literature on maternal PKU management and outcomes contextualizes the findings. The neonate, delivered at 38 weeks via cesarean section, exhibited low birth weight (2150 g), severe microcephaly (head circumference: 28 cm), microphthalmia, and septal heart defects. Maternal dietary non-adherence, beginning in late adolescence, contributed to significantly elevated phenylalanine levels during pregnancy (>20 mg/dL). Prenatal care was initiated in the 23rd week of gestation, delaying dietary intervention. The mother reported limited understanding of the teratogenic risks associated with poor dietary control, which was compounded by gaps in preconception counseling and care continuity. This case underscores the critical need for comprehensive preconception education and lifelong metabolic management for women with PKU. Early and sustained dietary adherence is essential to mitigate neonatal risks. Public health initiatives should prioritize access to preconception care, enhance patient education, and establish robust multidisciplinary support systems to optimize maternal and neonatal outcomes. Addressing barriers such as delayed care initiation and limited dietary support can significantly reduce the burden of maternal PKU syndrome.
母体苯丙酮尿症(PKU)是一种由苯丙氨酸羟化酶活性缺陷引起的代谢紊乱疾病,需要终身严格的饮食管理以防止有毒的苯丙氨酸积累。在怀孕期间,不坚持低苯丙氨酸饮食会导致母体PKU综合征,从而引发严重的新生儿并发症,包括小头畸形、先天性心脏缺陷和生长受限。尽管在代谢管理和孕前护理指南方面取得了进展,但坚持饮食管理仍然是一项重大挑战,尤其是在从儿科护理过渡到成人护理阶段的人群中。本病例报告探讨了母体PKU饮食不依从的临床后果,强调了孕前教育、代谢监测和多学科护理在预防不良新生儿结局方面的重要性。我们使用CARE指南,介绍了一名患有未经治疗的PKU的母亲所生男性新生儿的临床病程。分析纳入了母亲的饮食史、产前护理细节和新生儿结局。此外,对当前有关母体PKU管理和结局的文献进行回顾,将研究结果置于背景之中。该新生儿在38周时通过剖宫产出生,出生体重低(2150克),患有严重小头畸形(头围:28厘米)、小眼畸形和室间隔心脏缺陷。母亲从青春期后期开始饮食不依从,导致孕期苯丙氨酸水平显著升高(>20毫克/分升)。产前护理在妊娠第23周开始,延迟了饮食干预。母亲表示对饮食控制不佳所带来的致畸风险了解有限,孕前咨询和护理连续性方面的差距进一步加剧了这种情况。本病例强调了对PKU女性进行全面孕前教育和终身代谢管理的迫切需求。早期且持续的饮食依从对于降低新生儿风险至关重要。公共卫生举措应优先提供孕前护理、加强患者教育,并建立强大的多学科支持系统,以优化母婴结局。解决诸如护理开始延迟和饮食支持有限等障碍,可显著减轻母体PKU综合征的负担。