I really debated sharing this. I mean, honestly, I’m making fun of diseases!
There sure are a lot of them out there though. And some of have some really funny names too.
I should know. I suffer from a rare disease called Large Vessel Vasculitis. It’s an autoimmune order where your immune system attacks your own large blood vessels (like the aorta). It affects 1 out of every 100,000 people.
And that’s been my entrée into the wild and wonderful world of wackily-named syndromes and disorders. While waiting for my diagnosis for my rather blandly-named disease, I had to contend with the possibility that I might have Giant Cell Arteritis, or Churg Strauss Syndrome, or Henoch-Schönlein Purpura, or Goodpasture Syndrome.
I actually got quite into the world of rare diseases. And this blog post is the result.
Gallows humor, I guess.
So, what I’ve got here is 50 rare diseases with the most interesting names from this awesome list from NORD, the National Organization of Rare Disorders. Shall we get started?
- African Iron Overload – like it says, abnormally elevated levels of iron in the body, first identified and more common in Africa; AKA Bantu Siderosis
- Arterial Tortuosity Syndrome – like it says, the lengthening and twisting of arteries throughout the body
- Blue Diaper Disease – genetic disorder resulting in the incomplete breakdown of tryptophan in the intestines, causing bluish urine
- Blue Rubber Bleb Nevus Syndrome – characterized by lesions on the skin or just under that are often dark blue; AKA Bean Syndrome
- Bullous Pemphigoid – chronic autoimmune skin disorder featuring blisters, hives, and itching
- Cat Eye Syndrome – chromosomal anomaly causing colobomas, gaps in the iris below the pupil that makes the eyes appear catlike
- Complete DiGeorge Syndrome – the absence of a thymus at birth; contrasted with DiGeorge Syndrome, which means a merely underdeveloped one
- Cri du Chat Syndrome – a chromosomal anomaly where newborns’ cries sound like cats’ meowing
- Dandy Walker Malformation – a congenital defect affecting the cerebellum; named for two doctors who studied it extensively; AKA Luschka-Magendie Foramina Atresia
- Duane Syndrome – a congenital eye movement disorder; AKA Duane Radial Ray Syndrome, Duane's Retraction Syndrome, Stilling-Turk-Duane Syndrome
- Fatal Familial Insomnia – like it says, a genetic disorder that keeps sufferers from sleeping and which can even lead to death
- Floating Harbor Syndrome – genetic condition with a number of different symptoms; named for the two hospitals where it was first discovered, Boston Floating Hospital and Harbor General Hospital in California
- Fragile X Syndrome – a chromosomal anomaly where the X chromosome is damaged, resulting in many various symptoms
- Geographic Tongue – inflammation of the tongue with a map-like pattern (if you have a good imagination); AKA Wandering Rash of the Tongue
- Goodpasture Syndrome – autoimmune disorder featuring inflammation of the kidneys and excessive bleeding into the lungs; named after Dr. Earnest Goodpasture, its discoverer
- Grover’s Disease – characterized by temporary small red lesions, typically on the chest and back; AKA Transient Acantholytic Dermatosis
- Hailey-Hailey Disease – genetic disorder featuring rashes and blisters on the neck, armpits, skin folds and genitals; AKA Benign Chronic Familial Pemphigus
- Hairy Cell Disease – blood cancer characterized by thin, hair-like projections on B lymphocytes (a type of white blood cell); AKA Leukemic Reticuloendotheliosis
- Hairy Tongue – lengthening and overgrowth of the bumps on your tongue, forming a brown or black coating
- Harlequin Ichthyosis – genetic skin disorder where newborn is covered with plates of thick skin that crack and split; AKA Harlequin Fetus, Harlequin Baby Syndrome
- Imperforate Anus – absence or abnormal location (vagina, bladder, etc.) of the anus
- Jumping Frenchman of Maine – neurological disorder featuring an unusually extreme startle response; first seen in a community of French-Canadian lumberjacks
- Kabuki Syndrome – characterized by distinctive facial features, suggesting the makeup of a Kabuki actor; hence AKA Kabuki Makeup Syndrome
- Leprechaunism – an abnormal resistance to insulin, causing short stature and unusual facial characteristics, suggestive of a leprechaun
- Locked-In Syndrome – neurological disorder where the patient is completely paralyzed but conscious
- Lymphocytic Infiltrate of Jessner – characterized by lesions on the skin caused by a buildup of white blood cells; AKA Jessner-Kanof Lymphocytic Infiltration
- Maple Syrup Urine Disease – genetic disorder where urine and earwax smell like maple syrup; AKA Branched-Chain Ketoacid Dehydrogenase Deficiency
- NORSE (New Onset Refractory Status Epilepticus) – continuous seizures that seemingly come from nowhere
- Palmoplantar Pustulosis – like it says (if you know Latin, that is), characterized by blisters on the palms of the hand and feet; AKA PPP
- Pentalogy of Cantrell – set of five birth defects that appear together, affecting the heart, lungs, bones & many other parts of the body; AKA Cantrell Deformity
- Prader-Willi Syndrome – genetic disorder featuring an insatiable appetite; subject of actress Mayim Bialik’s PhD dissertation; AKA Willi-Prader syndrome, Prader-Labhart-Willi syndrome, Hypogonadism Hypotonia Hypomentia Obesity (HHHO)
- Prune Belly Syndrome – congenital absence of the abdominal muscles, resulting in a severely wrinkled abdomen; AKA Eagle-Barrett Syndrome
- Pseudo Hurler Polydystrophy – genetic disorder resulting in a build-up of toxic materials in the body’s cells due to enzyme deficiencies; a milder form of Hurler Syndrome
- Pure Autonomic Failure – abnormal accumulation of a certain protein in autonomic nerves, resulting in low blood pressure upon standing up; AKA Bradbury-Eggleston syndrome
- Q Fever – infection common among farmworkers and others who work with animals
- Schnitzler Syndrome – autoimmune disorder featuring a red rash; not to be confused with Schindler Disease, Schinzel Syndrome, or …
- Shprintzen Goldberg Syndrome – `a disease of connective tissue, with symptoms resembling Marfan Syndrome (which Lincoln may have had); AKA Marfanoid-Craniosynostosis Syndrome
- Sprengel Deformity – congenital condition where one shoulder blade is higher than the other; AKA Scapula Elevata
- Stiff Person Syndrome – characterized by progressive muscle stiffness and spasms
- Sweet Syndrome – a buildup of neutrophils (white blood cells) in the skin, resulting in fever and a rash; identified by a Dr. Robert Sweet
- Tarsal Tunnel Syndrome – the foot’s version of carpal tunnel syndrome
- Tethered Cord Syndrome – like it says, a set of symptoms caused by the spinal cord’s becoming attached to the spine, limiting its movement & causing a number of different symptoms
- Tetralogy of Fallot – set of four heart defects that appear together; characterized by a blue tint to the skin
- Timothy Syndrome – genetic disorder primarily affecting the heart; often results in webbed fingers and toes; named after Dr. Katherine Timothy, who first described it
- Tooth and Nail Syndrome – genetic condition causing absence/deformation of teeth and small/undeveloped finger and toe nails
- Tropical Sprue – tropical disease causing the intestines to not absorb enough nutrients
- Usher Syndrome – genetic disorder causing deafness and blindness; named for Dr. Charles Usher, who studied it
- Visual Snow Syndrome – neurological condition making one’s visual field resemble “snow” on an old TV; AKA Persistent Positive Visual Phenomena
- Wandering Spleen – weakness or absence of the ligaments holding the spleen in; AKA Displaced, Drifting, and Floating Spleen
- Whipple Disease – very similar to Tropical Sprue (and also know as Secondary Non-Tropical Sprue); first described by Nobel Prize winner Dr. George Hoyt Whipple
No comments:
Post a Comment