rare disease day crossword

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Across
  1. 5. Diagnosis doesn’t have to be - - - - is the slogan of Shire initiative
  2. 7. Genetic disease characterized difficulty of movement, coarse facial features, hernias, Respiratory infection and sometimes mental retardation
  3. 9. treatment for Fabry disease
  4. 11. Genetic disease characterized by low platelets, low blood count, enlargement of spleen and liver and bone pain
  5. 13. twenty? fifty? or ninety? percent of RD affect children?
  6. 15. latest rare disease treatment added to Biologix’s portfolio
  7. 19. Biologix partner with rare diseases products
  8. 20. Overproduction of growth hormone causing abnormal growth of the hands, feet, and face
  9. 23. spreading info and knowledge
  10. 24. (how many?) thousand is the approximate number of different rare diseases
  11. 25. Raise and Join - - - - in support or RD day
  12. 27. Hunter, Fabry and Gaucher diseases are characterized by a deficient or malfunctioning (what)?
  13. 29. treatment for Gaucher disease
Down
  1. 1. Genetic disease characterized by pain, cardiovascular, renal and cerebral events and a relatively young age
  2. 2. the science of genes, genetic variation, and heredity in living organisms
  3. 3. RD day occurs in which month?
  4. 4. a major symptom of nephropathic cystinosis in children
  5. 6. twenty? Forty five? seventy? or eighty? percent of rare disease are caused by a faulty gene
  6. 8. A disease or disorder is defined as rare in Europe when it affects fewer than 1 in 2000: True (T) or False (F)
  7. 10. Biologix Partner with rare diseases products
  8. 12. the star of 2016’s rare disease day poster
  9. 14. A "gene" that u wear as pants
  10. 16. carries our genes, is constituted of DNA and present in 23 pairs in the cells
  11. 17. Hunter syndrome is also called Mucopolysaccharidoses MPS1, MPS2 or MPS6?
  12. 18. a medical condition in which the lens of the eye becomes opaque, could be caused by Cerebrotendinous xanthomatosis
  13. 21. treatment for Hunter syndrome
  14. 22. treatment for IGF-1D also known as short stature
  15. 25. join us in making the voice of rare disease ….
  16. 26. it can take on average (Five? Nine?) years before a person with a rare disease receives the right diagnosis
  17. 28. abbreviation of NeuroEndocrine Tumors