Early-onset Exfoliation Syndrome: A Literature Synthesis
نویسندگان
چکیده
منابع مشابه
Hyperreactio Luteinalis with early-onset HELLP syndrome: A case report
Introduction: Hyperreactio Luteinalis (HL) is a rare benign condition in pregnancy which is characterized by bilaterally multicystic ovarian enlargement containing theca lutein cysts caused by increased production of hCG. HL is mostly associated with hydatidiform mole and multiple pregnancies. Correspondence: Azin Alavi, ...
متن کاملEarly Onset of Fragile X Associated Tremor and Ataxia Syndrome: A Case Report from Iran
Background: Different alleles of Fragile X Mental Retardation1 (FMR1) gene with separate molecular etiologies cause Fragile X Syndrome (FXS) and Fragile X-associated Tremor and Ataxia Syndrome (FXTAS). Premutation alleles with 55 to 200 repeats in the FMR1 gene lead to FXTAS. It is carried by 1 in 209 women and 1 in 430 men. FXTAS commonly appears in 50- to 70-year-old adults. Case Presentatio...
متن کاملEARLY ONSET BENIGN OCCIPITAL EPILEPSY (PANAYIOTOPOULOS SYNDROME): REPORT OF A CASE
ABSTRACT Seizure disorders are the most common neurological illnesses in infants and children. Presented is an 8 year old boy with nocturnal vomiting episodes, found to have EEG characteristics of early onset benign occipital epilepsy, better known as Panayiotopoulos syndrome.
متن کاملhyperreactio luteinalis with early-onset hellp syndrome: a case report
introduction: hyperreactio luteinalis (hl) is a rare benign condition in pregnancy which is characterized by bilaterally multicystic ovarian enlargement containing theca lutein cysts caused by increased production of hcg. hl is mostly associated with hydatidiform mole and multiple pregnancies. correspondence: azin alavi, md. hormozgan feritiliy and infertility research center, hormozgan univers...
متن کامل[Early-onset sarcoidosis/Blau syndrome].
Familial Blau syndrome and sporadic early-onset sarcoidosis (EOS) are both systemic granulomatous diseases evoked by the spontaneous activation of mutated NOD2. In Japan, the R334W amino acid substitution is more frequently identified, whereas the R334Q mutation is rare and, in contrast to western countries where disease causing mutations are typically hereditary, most Japanese cases derive fro...
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: Journal of Glaucoma
سال: 2021
ISSN: 1057-0829
DOI: 10.1097/ijg.0000000000001784