Hypergonadotropic hypogonadism in spinocerebellar ataxia type 2: A case report

Keyphrases

• Spinocerebellar Ataxia Type 2 100%
• Hypergonadotropic Hypogonadism 100%
• Cerebellar Ataxia 66%
• Clinical Spectrum 66%
• Hypogonadism 66%
• Pons 33%
• Older Men 33%
• Brain Magnetic Resonance Imaging 33%
• Left-handed 33%
• Cerebellum 33%
• Genotype 33%
• Infertility 33%
• Spinocerebellar Ataxia 33%
• Neurologic Signs 33%
• Genetic Analysis 33%
• Atrophy 33%
• Clinical Manifestations 33%
• Magnetic Resonance Imaging Scan 33%
• Neurologic 33%
• Azoospermia 33%
• Impaired Balance 33%
• Academic Medical Centers 33%
• Secondary Sexual Traits 33%
• Accompanying Symptoms 33%
• Multisystem Involvement 33%
• Hand Tremor 33%
• Neurological Manifestations 33%
• Triplet Repeat Expansion 33%
• Trinucleotide Repeat Diseases 33%
• Orchidometry 33%
• Variable Phenotype 33%
• Micropenis 33%
• Progressive Ataxia 33%
• CAG Triplet 33%
• Hereditary Ataxia 33%
• Testicular Size 33%
• Walking Balance 33%

Medicine and Dentistry

• Hypergonadotropic Hypogonadism 100%
• Spinocerebellar Ataxia 100%
• Disease 66%
• Cerebellar Ataxia 66%
• Hypogonadism 66%
• Magnetic Resonance Imaging 33%
• Neurologic Disease 33%
• Physical Examination 33%
• Genetic Analysis 33%
• Allele 33%
• Laboratory Test 33%
• Cerebellum 33%
• Balance Impairment 33%
• Pons 33%
• Ataxia 33%
• Neurologic Finding 33%
• Hand Tremor 33%
• Azoospermia 33%
• Trinucleotide Repeat 33%
• Hereditary Ataxia 33%
• Micropenis 33%