22q11.2 deletion syndrome

22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency.

Diabetes mellitus

A group of abnormalities characterized by hyperglycemia and glucose intolerance.


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(per page)
PMID (PMCID)
28018696
(5149642)
 OTHER
Alagille Syndrome: A Case Report Highlighting Dysmorphic Facies, Chronic Illness, and Depression.
Bresnahan JJ, Winthrop ZA, Salman R, Majeed S.
Case Rep Psychiatry. 2016;2016:1657691.
Alagille syndrome shares multiple phenotypic variants of other congenital or chronic childhood illnesses such as DiGeorge syndrome, Down syndrome, spina bifida, type 1 diabetes mellitus, and cystic fibrosis.