porphyria (Also porphyrias) : Related Words Words similar in meaning to porphyria
- porphyria«
- porphyric«
- acute porphyria«
- uroporphyrin«
- porphyrin«
- congenital disease«
- protoporphyria«
- heme«
- genetic abnormality«
- congenital erythropoietic porphyria«
- hereditary disease«
- symptom«
- hereditary condition«
- acute intermittent porphyria«
- inherited disorder«
- acute attack«
- genetic disorder«
- coproporphyrinogen«
- folkloric vampire«
- inherited disease«
- coproporphyria«
- heme arginate«
- genetic disease«
- genetic defect«
- hematin«
- patient«
- porphyria cutanea tarda«
- attack«
- george iii«
- normosang«
- skin«
- disease«
- treatment«
- liver«
- vampire«
- variegate porphyria«
- hereditary coproporphyria«
- aip«
- cep«
- urine«
- enzyme«
- accumulation«
- seizure«
- gabapentin«
- porphyria testing«
- nervous system«
- oral contraceptive«
- heme precursor«
- panhematin«
- substance«
- blood«
- purple secret«
- pseudoporphyria«
- skin disease«
- genetic carrier«
- abdominal pain«
- drug«
- sufferer«
- king george iii«
- felix hoppe«
- king george«
- epp.«
- hypertrichosis«
- seyler«
- status epilepticus«
- depression«
- sample«
- deficiency«
- mental illness«
- photosensitivity«
- aetiology«
- type«
- hepatocellular carcinoma«
- neuropathy«
- underlying mechanism«
- anxiety«
- catatonia«
- severe symptom«
- diagnosis«
- maria«
- barbiturate«
- sign«
- liver disease«
- energy level«
- blister«
- bone marrow«
- paper«
- psychosis«
- explanation«
- stool«
- confusion«
- pain«
- wide constellation«
- which—the«
- vampire report«
- vagal nerve dysfunction«
- urine estimation«
- urinary pbg«
- underlying mechanism result«
- tin mesoporphyrin«
- three—are«
- symptom control«
- sensitive blistering rash«
- rifabutine«
- rare ala dehydratase deficiency«
- puberty genetic carrier«
- psychiatric problems«
- proto oxidase«
- prominent lesion«
- porphyrin study«
- porphyrin secretion«
- porphyrin profile«
- porphyrin pathway«
- porphyria seizure«
- porphyria claim«
- physician archie cochrane«
- p450 liver cytochrome«
- other typical risk factor«
- other psychiatric symptom«
- mother/son psychiatrist team«
- milder skin disease«
- memoir paula«
- m. guttmacher«
- local skin damage«
- latent post«
- l. illis«
- intravenous heme«
- innate heme production«
- immediate photosensitivity«
- hereditary tyrosinemia type i.«
- heme function«
- greek πορφύρα«
- grade beta carotene«
- gold antirheumatic agent«
- foreign affair luís pinto«
- fluorescence typical«
- exhumation test«
- european metamorphosis legend«
- erythropoietic porphyria«
- erythropoietic form«
- erosive skin disease«
- episodic crisis«
- dysfunctional enzymes—have«
- dutch physician barend stokvis«
- detailed medical correspondence«
- cyclical attack«
- chronic porphyrias«
- certain antiretroviral medication«
- basic biochemical test«
- amino levulinic acid dehydratase deficiency«
- acute porphyric crisis«
- acute porphyrias«
- acute porphyria syndrome«
- acute neurological attack«
- acute neurologic attack«
- acute attack pass«
- avoidance«
- hallucination«
- nausea«
- hormone«
- vesiculo«
- urine screening test«
- therapeutic scope«
- severe shortening«
- seizures«
- porphyric hemophilia«
- porphyria variegata«
- peripheral nervous system involvement«
- offending symptom«
- most seizure medication«
- incidence report«
- hypoganglionosis«
- hepatitis c. treatment«
- granddaughter princess charlotte«
- fertility hormone«
- excess porphyrin«
- discolored teeth«
- diagnostic suspicion«
- daughter princess feodora«
- coproporphyrin«
- characteristic blistering«
- careful medication review«
- biochemist david dolphin«
- axonal nerve deterioration«
- abdominal spasm«
- % infusion«
- intermediate«
- skin lesion similar«
- severe photosensitivity«
- porphyrin synthesis pathway«
- overt psychosis«
- mixed porphyria«
- minimal systemic absorption«
- cutaneous porphyria«
- alert bracelet«
- additional tests«
- uroporphyrins«
- toxic precursor«
- term prophylaxis«
- photoactive molecule«
- minor knock«
- many psychiatrist«
- dominant protoporphyria«
- burning«
- werwolves«
- severe skin disease«
- severe dysfunction«
- progressive disappearance«
- original werewolf«
- heme biosynthetic pathway«
- grandson prince william«
- erythropoietic«
- certain antibiotic«
- c.e.p«
- brown teeth«
- acute polyneuropathy«
- paula frías allende«
- motor neuropathy«
- intestinal pseudo«
- flupentixol«
- enzyme testing«
- curative drug«
- chronic psychiatric illness«
- chilean novelist isabel allende«
- central nervous system symptom«
- ala synthase«
- acute hepatic porphyria«
- coma«
- werewolf legend«
- vampire belief«
- triggers«
- madness«
- mutation«
- sunlight«
- sodium aurothiomalate«
- hepatoerythropoietic porphyria«
- acute mental illness«
- skin fragility«
- repeat testing«
- hepatic porphyria«
- abnormal hair growth«
- erosion«
- hormonal fluctuation«
- rifapentine«
- hospital lab«
- ergot derivative«
- postgraduate medical journal«
- mercury-«
- light result«
- variegate«
- partial deficiency«
- inappropriate antidiuretic hormone«
- glipizide«
- skin appendage«
- most kind«
- low blood sodium«
- gliclazide«
- alad«
- porphobilinogen«
- glucose solution«
- glimepiride«
- empirical treatment«
- worldwide prevalence«
- heme synthesis«
- selective interpretation«
- rare manifestation«
- insufficient production«
- chronic neuropathic pain«
- stool test«
- heme biosynthesis«
- glibenclamide«
- dihydroergotamine«
- nancy garden«
- primary liver cancer«
- francis willis«
- methysergide«
- retrospective diagnosis«
- low occurrence«
- ethosuximide«
- variable period«
- severe scarring«
- seizure control«
- such drug«
- regency crisis«
- primary manifestation«
- erythropoietic protoporphyria«
- acute mania«
- pain treatment«
- iii«
- condition«
- sulfadiazine«
- residual activity«
- hyponatraemia«
- eye abnormality«
- ergometrine«
- prussia«
- vampire legend«
- thiopental«
- skin manifestation«
- sulfasalazine«
- essential constituent«
- encopresis«
- decreased production«
- systemic treatment«
- predominant«
- drug exposure«
- classic case«
- trimethoprim/sulfamethoxazole«
- siadh«
- primidone«
- false negative result«
- depressive psychosis«
- tolerable level«
- etomidate«
- nevirapine«
- nitrofurantoin«
- porphyra«
- severe episode«
- phototoxicity«
- methyldopa«
- exhaustive analysis«
- main precursor«
- griseofulvin«
- flutamide«
- seizure medication«
- fenfluramine«
- reference laboratory«
- neurological complication«
- voriconazole«
- symptom due«
- intussusception«
- pentazocine«
- rapid heart rate«
- staff time«
- king nebuchadnezzar«
- ileus«
- respiratory paralysis«
- preventive treatment«
- iron overload«
- mental derangement«
- sunlight exposure«
- sulfonylurea«
- lundbeck«
- ergotamine«
- emperor william ii«
- normal skin«
- disulfiram«
- vlad iii«
- valproate«
- nerve conduction study«
- biochemical analysis«
- polyneuropathy«
- notion«
- classic symptom«
- alcohol«
- crisis«
- oral ingestion«
- elevated blood pressure«
- specific mutation«
- major symptom«
- notable cases«
- hemochromatosis«
- chloroquine«
- carbohydrate diet«
- cellular metabolism«
- rare variant«
- sleeve shirt«
- electroshock therapy«
- fluconazole«
- cimetidine«
- psychiatric symptom«
- magnesium sulfate«
- phenobarbital«
- progestogen«
- physical sign«
- rifampicin«
- hyponatremia«
- psychotropic drug«
- paresis«
- antifungal«
- osteosclerosis congenita«
- achondroplasia«
- otosclerosis«
- congenital pancytopenia«
- congenital megacolon«
- congenital afibrinogenemia«
- polygenic disorder«
- polygenic disease«
- dwarfism«
- monogenic disorder«
- monogenic disease«
- hepatolenticular degeneration«
- autosomal recessive disease«
- autosomal recessive defect«
- autosomal dominant disorder«
- autosomal dominant disease«
- nevoid elephantiasis«
- ichthyosis«
- lactase deficiency«
- inborn error of metabolism«
- marble bones disease«
- maple syrup urine disease«
- lactose intolerance«
- muscular dystrophy«
- dystrophy«
- juvenile amaurotic idiocy«
- milk intolerance«
- pachyderma«
- osteopetrosis«
- oligodontia«
- oligodactyly«
- nanism«
- mucopolysaccharidosis«
- hyperbetalipoproteinemia«
- chondrodystrophy«
- branched chain ketoaciduria«
- achondroplasty«
- abetalipoproteinemia«
- xeroderma«
- myotonia atrophica«
- phenylketonuria«
- galactosemia«
- osteogenesis imperfecta«
- familial hypercholesterolemia«
- thalassaemia«
- sickle-cell anaemia«
- drepanocytic anaemia«
- crescent-cell anaemia«
- sickle-cell disease«
- sickle-cell anemia«
- pancreatic fibrosis«
- cystic fibrosis«
- infantile amaurotic idiocy«
- myotonic muscular dystrophy«
- myotonic dystrophy«
- neurofibromatosis«
- fibrocystic disease of the pancreas«
- malignant hyperthermia«
- drepanocytic anemia«
- crescent-cell anemia«
- diabetes«
- thalassemia«
- von Recklinghausen's disease«
- severe combined immunodeficiency disease«
- pseudohypertrophic dystrophy«
- oculopharyngeal muscular dystrophy«
- limb-girdle muscular dystrophy«
- distal muscular dystrophy«
- severe combined immunodeficiency«
- dysostosis multiplex«
- xerodermia«
- tyrosinemia«
- thrombasthenia«
- pycnodysostosis«
- mucoviscidosis«
- lysinemia«
- lipochondrodystrophy«
- gargoylism«
- 20th century variant«
- Fanconi's anaemia«
- Fanconi's anemia«
- Wilson's disease«
- Spielmeyer-Vogt disease«
- McArdle's disease«
- Hirschsprung's disease«
- Albers-Schonberg disease«
- Huntington's chorea«
- Mediterranean anaemia«
- Marfan's syndrome«
- Hurler's syndrome«
- Mediterranean anemia«
- Werdnig-Hoffman disease«
- Tay-Sachs disease«
- Steinert's disease«
- Sachs disease«
- Niemann-Pick disease«
- Hurler's disease«
- Huntington's disease«
- Gaucher's disease«
- Duchenne's muscular dystrophy«
- Becker muscular dystrophy«
- Tay-Sachs«
- SCID«
- PKU«
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