Another Deck Flashcards
Time of presentatoin and resolution of femoral ante version
Presents age 4-6
Resolves 10-13
Lateral talus OCDs are:
Less common than medial
Typically traumatic
Less likely to respond to non op management
Shallower than medial lesions
Extra abdominal Desmoid tumors
Wide resectoin
Does not metastasize
Estrogen receptor Beta positive
High association with FAP syndrome
RUNX2 is also known as
CBFA1
Gene mutatoin in cleidocranial dysplasia
If you see a locked plate on long bone with long working length think this type of bone healing
Endochondral
Indirect
Flexible and strong construct
BMPS signal through which molecules
SMADS
BMP target cells
Undifferentiated perivascular mesenchymal cells
This BMP is associated with fibrodysplasia ossificans progressiva
Bmp4
These things inhibit fracture healing
Nicotine
Quinolone
Cortisone
NSAIDs
Do you need to tissue Match osteochondral allografts?
Yes, cartilage is highly immunogenicity, so tissue matching is necessary
The major antigen in allograft is
Cell surface glycoproteins
T lymphocyte response
Cellular response, not humoral
Marrow cells incite the greatest response
Is DBM osteoinductive?
Yes but minimally
BMPS are preservered
What bone formation type happens in distraction osteogenesis
Endochondral occurs if low stability
If optimal stability, will be intramembranous
Optimal prophylactic radiation dose for HO preventoin
Single dose
600-700 rad
Recommended vitamin d dose for children
600mg/day
Recommended D dose for adults
750mg/day
Recommended D dose for adults over 50
1200-1500mg
Cancer risk of teriparatide
Increased sarcoma risk
Functions of PTH
- activates osteoblasts
Increases renal phosphate filtration
Jansen metaphyseal displasia
Dilantin effects on bone metabolism
Inhibits vitamin D metabolism
Fungal. Nail infections are associated with
Hypocalcemia
Pseudohyperparathyroidism
GNAS mtuatoin
Cellular response to PTH is defective
Defect in CAMP system
Amy.oidosis
Beta microglobulin Carpal tunnel syndrome Arthropathy Pathological fractures Congo red stain
Physis zone affected by rickets
Provisional calficication
Disoriented and widened
Mutations in Hereditary vitamin D dependent rickets
Type 1: defect in renal 25 hydroxylase
Type 2: defect in receptor for 1,25D
Autosomal recessive
Familial hypophosphatemic rickets
X linked Phosphate wasting proximal renal tubular defect Normal calcium Low phos Low D3 Elevated alk phos
Treatment is phosphate supplementation and high dose D3
Elevated urinary phosphoethanolamine is diagnostic of
Hypophosphatasia
Methotrexate
Folate analog
Inhibits purine metabolism
Me Alon ate pathway
Leflunomide
Inhibits pyrimidine synthesis
Stop for surgery
Hydroxxychloroquine (plaquenil)
Inhibits toll like receptor TLR9
Need ophthalmology evaluation annually
Anakinra
Anti-IL1 antibody
Diagnostic criteria JIA
6 weeks joint swelling in someone younger than 16 years