Chakraborty Soumalya, Kaur Ravneet, Patra Bijoy, Meena J P, Kabra S K, Kabra Madhulika, Gupta Neerja
Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110029, India.
Pediatric Intensive Care, Department of Pediatrics, ABVIMS & Dr. RML Hospital, New Delhi, 110001, India.
Indian J Pediatr. 2025 Jan;92(1):70-72. doi: 10.1007/s12098-024-05124-y. Epub 2024 May 4.
Lysinuric protein intolerance (LPI) is an inborn metabolic error caused by cationic amino acid transport defects. The disease has a significant degree of phenotypic variation, with no confirmed genotype-phenotype correlation. Because it presents with symptoms similar to far more common diseases, the diagnosis is often missed, resulting in increased morbidity and mortality. This case series describes three examples of LPI with pulmonary, neurological, and immunological manifestations, emphasising the importance of keeping this disorder on the differential list. Appropriate metabolic and genetic testing is important in providing the correct diagnosis and timely care in such cases.
赖氨酸尿性蛋白不耐受症(LPI)是一种由阳离子氨基酸转运缺陷引起的先天性代谢紊乱。该疾病具有显著程度的表型变异,尚无确诊的基因型-表型相关性。由于其表现出与更为常见疾病相似的症状,诊断常常被遗漏,导致发病率和死亡率上升。本病例系列描述了三例具有肺部、神经和免疫表现的LPI,强调了在鉴别诊断中考虑这种疾病的重要性。在这类病例中,进行适当的代谢和基因检测对于提供正确诊断和及时治疗至关重要。