TY  - CHAP
M1  - Book, Section
TI  - Osteogenesis Imperfecta
A1  - Hay, Jr, William W.
A1  - Levin, Myron J.
A1  - Deterding, Robin R.
A1  - Abzug, Mark J.
PY  - 2017
T2  - Quick Medical Diagnosis & Treatment Pediatrics
AB  - Rare  genetic  connective  tissue  disease;estimated  incidence  is  1  in  12,000–15,000Characterized  by  multiple  and  recurrent  fracturesThere  are  several  forms  of  osteogenesis  imperfecta,  designated  type  I  to  type  XIITypes  I–V  are  the  result  of  autosomal  dominant  mutationsTypes  VI–XII  are  autosomal  recessiveEach  type  is  associated  with  a  mutation  of  a  different  gene,  varying  levels  of  severity,  and  a  range  of  characteristic  featuresThe  severe  fetal  type  (osteogenesis  imperfecta  congenita)  is  distinguished  by  multiple  intrauterine  or  perinatal  fractures  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1145457471
ER  -