Familial Mediterranean fever: clinical and genetic characterization in a mixed pediatric population of Jewish and Arab patients.

Keyphrases

• Familial Mediterranean Fever 100%
• Pediatric Population 100%
• Jewish Patients 100%
• Arab Cardiovascular Patients 100%
• Genetic Characterization 100%
• Clinical Characterization 100%
• M694V mutation 50%
• Ashkenazi Jews 25%
• Arab children 25%
• Arab 25%
• Jewish children 25%
• Amyloidosis 25%
• Counseling 12%
• North African Jews 12%
• Disease Severity 12%
• MEFV Gene 12%
• Genotype-phenotype Correlation 12%
• Pain Severity 12%
• Ethnic Origin 12%
• Family History 12%
• Homozygosity 12%
• Natural History 12%
• Severe Disease 12%
• Age of Onset 12%
• Clinical picture 12%
• Better Prognosis 12%
• Mixed Population 12%
• Clinical Treatment 12%
• Colchicine 12%
• Global Assessment 12%
• Clinical Manifestations 12%
• Polymerase Chain Reaction 12%
• Severe Course 12%
• Mutation Type 12%
• Arthritis 12%
• Fever 12%
• Turks 12%
• Disease Occurrence 12%
• Molecular Genetic Testing 12%
• Rational Basis 12%
• Hereditary Disease 12%
• Armenians 12%
• Genotype-phenotype 12%
• Uncommon mutation 12%
• Autosomal Recessive 12%
• Restriction Digestion 12%
• Abdominal Pain 12%
• Treating Physicians 12%
• Clinical Onset 12%
• DNA Variation 12%
• M694V 12%
• Correlation Study 12%
• Genotype Patterns 12%
• Digestion Method 12%
• Skin Eruption 12%
• Pleuritis 12%
• Familial Mediterranean Fever Patient 12%
• Skin Response 12%
• Mild Course 12%
• Exon 10 12%

Biochemistry, Genetics and Molecular Biology

• Genetics 100%
• MEFV 100%
• Amyloidosis 100%
• Genotyping 50%
• Prevalence 50%
• Genotype Phenotype Correlation 50%
• Homozygosity 50%
• Restriction Modification System 50%
• Exon 50%
• Autosomal Recessive Inheritance 50%
• Molecular Genetics 50%
• Polymerase Chain Reaction 50%

Neuroscience

• Amyloidosis 100%
• Exon 50%
• Colchicine 50%
• Restriction Endonuclease 50%
• Polymerase Chain Reaction 50%