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本文报道1例发-肝-肠综合征患儿的诊治经过。患儿，女，胎龄38周，出生体重1 700 g，11日龄，因“皮肤黄染6 d”于2019年1月就诊于济宁医学院附属医院，患儿头发色黄、细软稀疏、易脱落，先天性心脏病，顽固性腹泻，反复发热，体重增长缓慢，经治疗25 d，感染控制，但仍腹泻，家属要求出院。患儿3月龄时因肺部感染再次入院，患儿发育落后，营养不良，前额突出，眼距宽，鼻梁低平，肝大，顽固性腹泻，通过全外显子组测序显示患儿n SKIV2L基因存在c.2344delC（p.His782fs）纯合变异，其父母亲均是该位点变异的杂合携带者。患儿确诊为n SKIV2L基因变异致发-肝-肠综合征。患儿持续腹泻，反复感染，家属放弃治疗，生后4月龄死于感染。n “,”We here report the diagnosis and treatment of tricho-hepato-enteric syndrome in a female neonate. The 11-day-old patient, born at a gestational age of 38 weeks and with a birth weight of 1 700 g, was admitted to the Affiliated Hospital of Jining Medical University in January 2019 due to “skin stained yellow for 6 d”. She presented with yellow, thin, and sparse hair that was easy to fall off, intractable diarrhea, repeated fever, and slow weight gain, further complicated by congenital heart disease. After 25-days of treatment, the child\'s infection was under control, but still had diarrhea. The baby girl was discharge later on request of her parents, but readmitted at the age of 3 months due to pulmonary infection. Delayed development, malnutrition, prominent forehead, wide eye distance, low nasal bridge, hepatomegaly, and intractable diarrhea were also observed. Whole exome sequencing identified a homozygous mutation of c.2344delC(p.His782fs) in n SKIV2L gene in the baby, and both her parents were heterozygous carriers of the mutation at this site. She was diagnosed with n SKIV2L gene mutation-induced tricho-hepato-enteric syndrome. The patient suffered from sustained diarrhea and recurrent infection and died of infection at 4 months of age after her parents\' decision to withdraw treatment.n