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FMF
Familial Mediterranean Fever
Infancy, to under 20 years of age for the onset of the first symptoms. -
MKD-mild/moderate (aka HIDS)
Mevalonate Kinase Deficiency-mild/moderate, Hyperimmunoglobulinemia D with Periodic Fever Syndrome
>90% present with symptoms in infancy. -
TRAPS
Tumor Necrosis Factor (TNF) - Associated Periodic Syndrome (aka Familial Hibernian Fever)
Most first attacks occur by 3 years of age, and almost all begin by 20 years of age. A few have symptoms start later in life. -
PFAPA
Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis (PFAPA) – aka Marshall Syndrome
Early childhood, usually between 2-5 years of age. A few adult-onset cases are documented. Most teens outgrow it. -
MA, MKD-severe
Mevalonate Aciduria (MA), Mevalonate Kinase Deficiency-severe
Most present with symptoms at birth, or in early infancy. Most have facial features noted at birth.
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