RareDisease

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• AgeX and UCI to Research Huntington Disease Therapies
• Fastex Improves Range of Fabry Disease Diagnostic Tools
• Protalix BioTherapeutics Presents Fabry Disease Research Findings
• Fabry Disease
• Klinefelter Syndrome
• Searching for Help with Trisomy 13 (Patau Syndrome)?
• Síndrome de Klinefelter
• Rare Disease List
• Neurofibromatosis
• Trisomía 13
• Neurofibromatosis (Español)
• Enfermedad de Fabry
• Lynch Syndrome Symptoms, Treatment + Guide
• Síndrome de Lynch
• Huntington's Disease Symptoms, Treatment + Podcast
• Ehlers Danlos Syndrome, Hypermobile type (EDS) and related disorders
• Enfermedad de Huntington - Síntomas, Tratamientos y Podcast
• Síndrome de Ehlers Danlos, tipo hipermóvil (SEDh) y trastornos relacionados
• 22q Deletion Syndrome: Symptoms, Treatment + Podcast
• Síndrome de Deleción 22q
• Multiple Sulfatase Deficiency (MSD) Simple Guide + Podcast
• Fragile X Syndrome (FXS) Simple Guide + Podcast
• Duchenne Muscular Dystrophy
• VLCAD: Symptoms, Treatment + Podcast
• TANGO2: Simple Guide + Podcast
• 5p- Syndrome (Cri du Chat Syndrome)
• Hermansky-Pudlak Syndrome (HPS) Simple Guide + Podcast
• Charcot Marie Tooth Disease (CMT)
• Angelman Syndrome: Symptoms, Treatment + Podcast
• Galactosemia
• Prader-Willi Syndrome (PWS): Symptoms, Treatment + Podcast
• Neurofibromatosis Type 2 (NF2)
• CHARGE Syndrome (CHD7)