cystic fibrosis-gastritis-megaloblastic anemia syndrome
MONDO:0009062
A rare genetic disease reported in two siblings of consanguineous Arab parents and is characterized by cystic fibrosis, gastritis associated with Helicobacter pylori, folate deficiency megaloblastic anemia, and intellectual disability. There have been no further descriptions in the literature since 1991.
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View cystic fibrosis-gastritis-megaloblastic anemia syndrome on the outbreak map →Lubani Al Saleh Teebi syndrome
Lubani Al Saleh Teebi syndrome also known as cystic fibrosis-gastritis-megaloblastic anemia syndrome is a very rare autosomal recessive genetic disorder which consists of cystic fibrosis, helicobacter pylori-associated gastritis, folate-deficiency megaloblastic anemia and intellectual disabilities. This disorder was discovered when Lubani et al reported two siblings from consanguineous parents with the symptoms mentioned above in 1991. Since then, there have been no further reports of this syndrome in medical literature.
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.