1. Histidinuria is a rare genetic disorder that affects the body's ability to break down the amino acid histidine.
组氨酸尿症是一种罕见的遗传疾病，影响了身体分解氨基酸组氨酸的能力。

2. Babies born with histidinuria may experience developmental delays and intellectual disabilities if not treated early.
患有组氨酸尿症的婴儿如果不及早治疗，可能会出现发育迟缓和智力障碍。

3. The diagnosis of histidinuria is usually confirmed through urine tests and genetic testing.
组氨酸尿症的诊断通常通过尿液检测和基因检测来确认。

4. Treatment for histidinuria may involve dietary changes and supplementation with specific nutrients.
组氨酸尿症的治疗可能涉及饮食改变和补充特定营养素。

5. Parents of children with histidinuria should work closely with healthcare professionals to manage the condition effectively.
患有组氨酸尿症的孩子的父母应该与医疗专业人员密切合作，有效管理疾病。

6. Research is ongoing to better understand the underlying causes of histidinuria and develop more effective treatments.
正在进行研究，以更好地了解组氨酸尿症的潜在原因，并开发更有效的治疗方法。