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Summary
CHILDHOOD VASCULITIS DD
KAWASAKI DISEASE
611775
OMIM = Online Medalian Inheritance of Men
2331
19q13.2
Childhood vasculitis is difficult to diagnose because of the wide variation in the symptoms and signs [Barut K 2016]
Purpura
Schoenlein-Henoch
Granulomatosis with Polyangiitis (GPA)
Microscopic polyangiitis (MPA)
Polyarteritis nodosa (PAN)
Eosinophilic granulomatosis with polyangiitis (Churg-Strauss EGPA)
Giant cell arteritis (GCA)
Takayasu Arteritis (TAK)
symptoms
conjunctivitis
fever
onset, childhood
onset, infancy
petechiae
skin rash, eczematous or seborrhoic
laboratory finding
Literature
Lalovic Aet al.Cholesterol metabolism and suicidality in Smith-Lemli-Opitz syndrome carriersAm J Psychiatry161112123-21262004
Ciara Eet al.DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndromeClin Genet666517-5242004
Schimel AMMets MBThe natural history of retinal degeneration in association with cobalamin C (cbl C) diseaseOphthalmic Genet2719-142006