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PedAM

Pediatric Disease Annotations & Medicines




Disease alopecia
Phenotype C0009447|common variable immunodeficiency
Sentences 2
PubMedID- 25068407 We report a unique patient, a 14 year old male from lazio region, affected by common variable immunodeficiency associated with autoimmune manifestations (alopecia, onychodystrophy) and heterozygote for the s250c variant located in the sand domain of the autoimmune regulator gene protein.
PubMedID- 21936858 Frontal fibrosing alopecia in a patient with common variable immunodeficiency.

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