MCQ Book Questions

Q51240. Main symptoms of congenital erythropoi- etic porphyria is

Q51241. The probable cause of porphyria cutanea tarda is deficiency of

Q51242. The characteristic urinary finding in por- phyria cutanea tarda is

Q51243. Hereditary coproporphyria is caused due to deficiency of

Q51244. The enzyme involved in variegate por- phyria is

Q51245. Protoporphyria (erythrohepatic) is char- acterized by the deficiency of

Q51246. The amount of coproporphyrins excreted per day in feces is about

Q51247. The immunoglobulins are differentiated and also named on the basis of

Q51248. The immunoglobulins are classified on the basis of

Q51249. All immunoglobulins contain

Q51250. An immunoglobulin molecule always contains

Q51251. The number of hypervariable region in L chain is

Q51252. The number of hypervariable region in H chain is

Q51253. Type γ γ γ γ γ H chain is present in

Q51254. Type α H chain is present in

Q51255. Type µ H chain is present in

Q51256. Type δ δ δ δ δ H chain is present in

Q51257. Type ε H chain is present in

Q51258. A ‘J’ chain is present in

Q51259. A secretory protein T chain (T protein) is present in