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Articles by K. Maples
M113 BLEPHAROCHALASIS: A HEREDITARY ANGIOEDEMA-MASQUERADER. RECURRENT ANGIOEDEMA IN A 12 YEAR-OLD AFRICAN AMERICAN MALE
Blepharochalasis is a rare disorder involving periocular edema classically of the upper eyelid, but has also been described in the entire periocular tissue. The resultant edema may be mistaken for allergy or hereditary angioedema. Etiology is unclear, possibly inflammatory, with some cases involving IgA deposition in the dermis, as well as perivascular inflammatory cellular infiltrates. Age of presentation ranges from just prior to puberty through the 20’s.
P026 ACAAI PATCH TESTING MEMBER-SURVEY: PATCH TESTING & EFFECT OF TRAINING ON CONFIDENCE, ATTITUDE, & USAGE
Allergic Contact Dermatitis (ACD) affects ∼ 13 million people in the United States and is the fifth most common skin disease impacting children and adults. Patch Testing is the gold standard for diagnosing contact dermatitis. It is a safe, inexpensive procedure which more allergists have been performing over the last decade. To read this article in full you will need to make a payment ACAAI Member Login ACAAI Member, full access to the journal is a member benefit.
M320 A UNIQUE PRESENTATION OF MILK ALLERGY
Introduction Food allergy typically presents with classic signs and symptoms of immediate type hypersensitivity. We describe a male infant with no history of an acute reaction to food but rather an unusual constellation of symptoms which resolved once milk allergy was diagnosed and his diet adjusted. Case Description A 6-month-old African American male presented with FTT, developmental delay, spasticity, normocytic anemia (Hgb: 7.9gm/dL), erythroderma, ichthyosis and hypereosinophilia.
P252 Association of P21R and H159Y polymorphism with common variable immunodeficiency and protein losing enteropathy
To view the full text, please login as a subscribed user or purchase a subscription. Click here to view the full text on ScienceDirect. Many genes have been implicated in common variable immunodeficiency (CVID), including TNFRSF13C, which encodes B-cell activating factor receptor (BAFF-R). B-cell activating factor (BAFF) binds to its receptor (BAFF-R) and is essential to B-cell development. Most TNFRSF13C variants that have been reported were heterozygous or homozygous for the P21R missense variant.
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