RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58082298
T1 Osteopetrosis
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58082298
RD 2024/04/19
AB Heterogenous  genetic  disorder  resulting  in  increased  bone  mass  as  a  consequence  of  defective  bone  resorption.  Depending  on  the  mode  of  inheritance,  its  course  can  be  either  uniformly  fatal  with  pancytopenia,  recurrent  pathologic  fractures,  blindness,  and  other  neurologic  symptoms,  or  it  can  exist  in  a  much  milder  form  with  later  manifestation  and  favorable  prognosis.