Items | N (%) | P-value |
---|---|---|
Fragile X syndrome | 1365 (20) | Â |
Alzheimer’s disease | 1499 (21.9) |  |
Progeria | 1006 (14.7) | Â |
Duchenne muscular dystrophy | 1466 (21.4) | Â |
Crohn’s disease | 2164 (31.6) |  |
Niemann-Pick disease | 1029 (15) | Â |
Huntington disease | 1342 (19.6) | Â |
Cerebral palsy | 1758 (25.7) | Â |
Marfan syndrome | 1957 (28.6) | Â |
Phenylketonuria | 1165 (17) | Â |
Munchausen syndrome | 438 (6.4) | Â |
Sickle cell anemia | 2064 (30.2) | Â |
Down syndrome | 1070 (15.6) | 0.012 |
Acromegaly | 1077 (15.8) | Â |
Osteogenesis imperfect | 680 (9.9) | Â |
Pompe disease | 715 (10.5) | Â |
Schizophrenia | 322 (4.7) | Â |
Mucopolysaccharidosis | 1782 (26.1) | Â |
Gaucher disease | 1916 (28) | Â |
Halitosis | 857 (12.5) | Â |
Haemophilia | 1618 (23.7) | Â |
Craniodiaphyseal dysplasia | 1312 (19.2) | Â |
Glaucoma | 1438 (21) | 0.01 |
Neurofibromatosis | 1037 (15.2) | Â |
Achondroplasia | 874 (12.8) | Â |
Cystic fibrosis | 1482 (21.7) | Â |
Acquired immunodeficiency syndrome | 1317 (19.3) | 0.018 |
Fibromyalgia | 532 (7.8) | Â |