Difference between revisions of "Connective tissue diseases"

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===General===
===General===
*Rare.
*Rare.
*Numerous subtypes.
*Numerous subtypes - mild-to-severe symptoms/survival.
*May be misdiagnosed as child abuse.<ref name=pmid21716141>{{Cite journal  | last1 = Singh Kocher | first1 = M. | last2 = Dichtel | first2 = L. | title = Osteogenesis imperfecta misdiagnosed as child abuse. | journal = J Pediatr Orthop B | volume = 20 | issue = 6 | pages = 440-3 | month = Nov | year = 2011 | doi = 10.1097/BPB.0b013e328347a2e1 | PMID = 21716141 }}</ref>
*May be misdiagnosed as child abuse.<ref name=pmid21716141>{{Cite journal  | last1 = Singh Kocher | first1 = M. | last2 = Dichtel | first2 = L. | title = Osteogenesis imperfecta misdiagnosed as child abuse. | journal = J Pediatr Orthop B | volume = 20 | issue = 6 | pages = 440-3 | month = Nov | year = 2011 | doi = 10.1097/BPB.0b013e328347a2e1 | PMID = 21716141 }}</ref>
Clinical:
*+/-Blue sclerae.<ref name=pmid1202551>{{Cite journal  | last1 = Smith | first1 = R. | last2 = Francis | first2 = MJ. | last3 = Bauze | first3 = RJ. | title = Osteogenesis imperfecta. A clinical and biochemical study of a generalized connective tissue disorder. | journal = Q J Med | volume = 44 | issue = 176 | pages = 555-73 | month = Oct | year = 1975 | doi =  | PMID = 1202551 }}</ref>
*Multiple fractures.


===General===
===General===
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