Autosomal-recessive hyper-IgE syndrome (AR-HIES ... Because of multiple dentogenic foci as the likely cause, all teeth were extracted. Antibiotic therapy was given for almost 1 year and the ...

A similar but distinct syndrome was reported by Renner et al. (9), characterized by extremely elevated serum IgE, severe eczema ... and the failure of baby teeth to exfoliate.

IgA and IgE. A rare form of hyper-IgM syndrome, X-linked, is associated with ectodermal dysplasia (XHM-ED): the absence of hair, teeth or sweat glands. In a study in March Nature Immunology, ...

People with Hyper IgE Syndrome, or 'Job's Syndrome', suffer from devastating complications of skin, gut and lung infections caused by candida albicans and Staphylococcus aureus. We all have these ...

Scientists are learning more about STAT3 loss-of-function, autosomal dominant hyper-IgE syndrome – a complicated name for a horrible, extremely rare genetic disease affecting fewer than 1,000 ...

Examples include hyper-IgE syndrome, DOCK8 deficiency, PGM3 deficiency, Wiskott-Aldrich syndrome, IPEX syndrome, and Netherton syndrome. Particular characteristics, such as eczematous rashes ...

allergic airway inflammation and hyper-IgE Syndrome, or HIES. Loss of IL-6 signaling was known to cause an increase in inflammatory T helper 2, or Th2, cells. T helper cells act like generals, ...