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facial dysmorphism-immunodeficiency-livedo-short stature syndrome

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Facial dysmorphism-immunodeficiency-livedo-short stature syndrome is a rare genetic disease characterized by facial dysmorphism with malar hypoplasia and high forehead, immunodeficiency resulting in recurrent infections, impaired growth (with normal growth hormone production and response) resulting in short stature, and livedo affecting face and extremities. Immunological analyses show low memory B-cell and naïve T cell counts, decreased T cell proliferation, and reduced IgM, IgG2 and IgG4 titers. Patients do not exhibit increased susceptibility to cancer.
Uniprot Description A syndrome characterized by mild facial dysmorphism, mainly malar hypoplasia, livedo on the skin since birth, and immunodeficiency resulting in recurrent infections. Growth impairment is observed during early childhood and results in variable short stature in adulthood.
Mondo Term and Equivalent IDs
MONDO:0014058:  facial dysmorphism-immunodeficiency-livedo-short stature syndrome
Orphanet:352712: 
UMLS:C3554576: