Mucopolysaccharides

Longa catenae Mucopolysaccharides iaculis moleculis reperiuntur in corpore saepe liquore circum coagmenta et mucus. Et magis ex nomine glycosaminoglycans.

Quando corpus non conteram mucopolysaccharides usque a conditione vocavit mucopolysaccharidoses (MPS) occurs. MPS ad catervam obnoxiae haereditatis de metabolismi perturbationes. Et populus non habes MPS, non sufficit, quod sit substantia (enzyme) opus erat, ut effringerent sugar moleculo catenis.

Formae autem MPS includit:

• Ego MPS (illest fulminis syndrome, illest fulminis, Scheie syndrome, Scheie syndrome)
• MPS II (Hunter syndrome)
• MPS III (Sanfilippo syndrome)
• MPS Libri IV (Morquio syndrome)

Glycosaminoglycans; IOCUS

Saint V, Abbas AK, Aster JC. Geneticae perturbationes. In Saint V, Abbas AK, Aster C, ed. Basis autem Robbins Cotran Pathologic Morbus. 9th ed. Lugduni: Gale Ecco, MMXV, Cap: V.

Pyeritz BE. Hereditario morbis nota TEXTUS. Et: Goldman Domino, Schafer AE, ED. Latin Goldman Cecilius,. 26 ad ed. Lugduni: Gale Ecco, MMXX, Cap CCXLIV.

C. Spranger. Mucopolysaccharidoses. In Kliegman RM, geme S. Lexicon, Oxford Blum, Shah parte Tasker RC Wilson KM, & xii. Cicero Book of Pediatrics. 21 ad ed. Lugduni: Gale Ecco, MMXX, Cap: CVII.