1256 Narcolepsy Type 2 in a Pediatric Patient with Auto-Immune Disease
نویسندگان
چکیده
منابع مشابه
Auto-Immune Addison\'s Disease Associated with Hyperprolactinemia
SUMMARY Three cases ofauto-immune addison's disease are reported in association with hyperprolactilinemia. All of them had galactorrhea. In three cases complete resolution of hyperprolactitinemia occurred with corticosteroid replacement. We suggest that hyperprolactinemia was due to cortisol deficiency operating directly or indirectly at the level of the pituitary.
متن کاملIVIG Anaphylaxis in a patient with Common variable immune deficiency disease (CVID).
Common variable immune deficiency disease (CVID) is one of the most common primary immunodeficiency disorders. It causes reduction of immunoglobulin levels and specific antibodies production and enhancement of recurrent and chronic infections risk, especially respiratory infections and gastrointestinal tracts. Here, we report a case of CVID in a 3 years old male with recurrent hospitalizations ...
متن کاملinsulinoma in a patient with type 2 diabetes mellitus.
insulinoma in a patient with pre-existing diabetes is extremely rare. only a small number of cases have been reported all over the world. we report a case of insulinoma in a patient with type 2 diabetes. a 63-year-old female was diagnosed to have diabetes mellitus six years ago, she was given metformin and sulphonylurea to control her glycemia, she had adequate glycemic control for many years, ...
متن کاملNarcolepsy as an Immune-Mediated Disease
Narcolepsy is a neurological disorder characterized by excessive daytime sleepiness, cataplexy, hypnagonic hallucinations, sleep paralysis, and disturbed nocturnal sleep patterns. This disease is secondary to the specific loss of hypothalamic hypocretin (orexin)-producing neurons in the lateral hypothalamus. An autoimmune basis for the disease has long been suspected based on its strong associa...
متن کاملCholelithiasis in a patient with type 2 Gaucher disease.
Gaucher disease is an autosomal recessively inherited lysosomal storage disease in which a deficiency of glucocerebrosidase is associated with the accumulation of glucocerebroside in reticuloendothelial cells. Clinically, 3 types of Gaucher disease have been defined on the basis of the presence or absence of neurological symptoms. The frequency of gallbladder involvement is reportedly greater i...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Sleep
سال: 2020
ISSN: 0161-8105,1550-9109
DOI: 10.1093/sleep/zsaa056.1250