Congenital cataracts in two siblings with Wolfram Syndrome

Keyphrases

• Congenital Cataract 100%
• Wolfram Syndrome 100%
• Optic Atrophy 80%
• Early childhood 60%
• Diabetes Insipidus 60%
• Childhood Cataract 60%
• Deafness 40%
• Compound Heterozygous mutation 40%
• Type 1 Diabetes Mellitus (T1DM) 20%
• Genetic Analysis 20%
• Autosomal Recessive 20%
• Mellitus Diabetes 20%
• Hearing Impairment 20%
• Differential Diagnosis 20%
• Cataract 20%
• Congenital Sensorineural Hearing Loss 20%
• Single-point mutation 20%
• Genetic Syndromes 20%
• Non-insulin-dependent Diabetes Mellitus (NIDDM) 20%
• Methods Observational 20%
• WFS1 Gene 20%
• WFS1 20%

Medicine and Dentistry

• Congenital Cataract 100%
• Wolfram Syndrome 100%
• Cataract 66%
• Optic Nerve Atrophy 50%
• Hearing Impairment 33%
• Genetic Analysis 16%
• Diabetes Insipidus 16%
• Differential Diagnosis 16%
• Genetic Disorder 16%
• Autosomal Recessive Inheritance 16%
• Sensorineural Hearing Loss 16%
• Insulin Dependent Diabetes Mellitus 16%