Auriculotemporal's syndrome in three siblings and literature review

نویسندگان

  • Masoud Grouhi
  • Mohammed Alshehri
چکیده

The skin is one of the target organs that are most often involved in food hypersensitivity reactions. Clinical manifestations of food hypersensitivity in the skin range from symptoms of atopic dermatitis, urticaria, angioedema to dermatitis herpetiformis, and a masquerader of food allergy, the Frey’s syndrome. All present with typical skin manifestations of their foodallergic reactions. Three cases of Frey’s syndrome (auriculotemporal) are presented in three children from the same family: two girls and one boy. The patients presented with a history of facial erythema in cheeks after eating different foods. Food radioallergosorbant (RAST) and percutaneous skin testing were, both, negative. Skin rash was reproduced in the clinic after oral challenge.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

CONGENITAL PERMANENT DIABETES MELLITUS WITH HYPOP LASIA OF THE PANCREAS: REPORT OF 2 CASES AND REVIEW OF THE LITERATURE

Two siblings (a girl and a boy) with intrauterine growth retardation and earlyonset insulin dependent diabetes mellitus, who had a clinical syndrome consistent with' congenital pancreatic hypoplasia will be reported.

متن کامل

USHER\'S SYNDROME REVISITED

Usher's syndrome is a genetically inherited autosomal recessive disorder resulting in the double handicap of deafness and progressive blindness, known as retinitis pigmentosa. The disease is also associated with psychoses, mental retardation, and other major neurophysiological changes. It appears to be more common among Jewish individuals and consanguinous marriages. While it is rare in th...

متن کامل

Acquired Unilateral Nevoid Telangiectasia Syndrome: A Case Report and Review of Literature

Unilateral nevoid telangiectasia syndrome (UNTS) can be classified into two major categories: congenital and acquired. There have been reports showing an increase in skin estrogen and progesterone receptors in patients with this syndrome. We report a male patient with acquired unilateral nevoid telangiectasia syndrome without any associated physiological or pathological conditions.<...

متن کامل

FAMILIAL COLLOID CYST OF THE THIRD VENTRICLE: A CASE REPORT AND REVIEW OF THE LITERATURE

Familial colloid cyst of the third ventricle is very rare. This is one of the two largest families reported and the first in which all affected members are siblings. One asymptomatic sister was found by screening, emphasizing the value of screening. A brother and two sisters from a family consisting of three brothers and three sisters who were diagnosed as having colloid cyst of the third v...

متن کامل

Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, mental retardation, hypotonia, functionally deficient gonads, and uncontrolled appetite leading to extreme obesity at an early age. Patients with this condition require multidisciplinary medical care, which facilitates a significant improvement in quality of life. PWS is the first human disorder to be attributed t...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2015