neonatal constitutional diarrhea
Types
congenital chloride diarrhea (DIAR1, MIM.214700, 7q22-q31.1)
- congenital chloride diarrhea (DIAR1) is caused by mutation in the SLC26A3 gene (MIM.126650) on chromosome 7q31.
microvillus inclusion disease (DIAR2; MIMI.251850)
- microvillus inclusion disease is caused by mutation in the MYO5B gene (MIM.606540) on chromosome 18q21
-
syndromic form of congenital secretory sodium diarrhea (DIAR3, MIM.270420), caused by mutation in the SPINT2 gene (MIM.605124)
malabsorptive congenital diarrhea (DIAR4; MIM.610370) caused by mutation in the NEUROG3 gene (MIM.604882) on chromosome 10q21.3;
congenital tufting enteropathy (DIAR5; MIM.613217) caused by mutation in the EPCAM (or TACSTD1) gene (MIM.185535).
See also
severe diarrhea
syndromic diarrhea