Neonatal Crohn’s disease with Oral ulcer as the first symptom caused by a compound heterozygote mutation in IL-10RA: a case report - Lv, Hongyan; Qiao, Baojun; Fang, Liyuan; Yang, Lihong; Wang, Qiuli; Wu, Sujing; Ren, Pengshun; Li, Lianxiang (Hereditas, 2019)
Keywords: Alleles; Antibiotics; Autoimmune diseases; Brief Report; Case reports; case studies; Crohn Disease - complications; Crohn Disease - genetics; Crohn's disease; Cytokines; Deoxyribonucleic acid; Diarrhea; Disease Susceptibility; DNA; Exanthema; Exons; Family medical history; Female; Fever; Fistula; Genes; Genetic Association Studies; Genetic mutation; genetic testing; girls; heterozygosity; Heterozygote; High-Throughput Nucleotide Sequencing; Humans; Infant, Newborn; Inflammatory bowel disease; Interleukin 10; Interleukin-10 receptor a; Interleukin-10 Receptor alpha Subunit - genetics; Laboratories; Maternal & child health; Missense mutation; Mutation; Neonate; Neonates; Next-generation sequencing; Oral ulcer; Oral Ulcer - complications; Oral Ulcer - diagnosis; Parents & parenting; patients; Phenotype; Ulcers; United States--US; Inflammatory bowel disease; Interleukin-10 receptor a; Neonate; Oral ulcer; Genetic mutation; Crohn’s disease