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Fig. 4 | Hereditas

Fig. 4

From: Neonatal Crohn’s disease with Oral ulcer as the first symptom caused by a compound heterozygote mutation in IL-10RA: a case report

Fig. 4

The patient carries one heterozygous mutation, c. 537G > A, P. (Thr 179 =), in exon 4 of the IL-10RA gene, which is a synonymous mutation (a, arrow). Her father has no abnormalities in this coding region of the IL-10RA gene (b). However, her mother carries one heterozygous mutation, c.537G > A, P. (Thr 179 =), in exon 4 of the IL-10RA gene (c, arrow)

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Hereditas

ISSN: 1601-5223

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