Collagen defects Flashcards
Osteogenesis Imperfecta
Bone=type 1 coll embedded in CaPh matrix
Muts of type 1 coll, precoll alpha1 chain genes
Most clinical severe phenotypes form substitute of inverted glycine
3x helix forms C to N term: gly mutations near C term = more deleterous; N term permits substantial 3x helix formation
Ranged severity: perinatal death - mild dispostion to fractures
Clin= skl defects, fractures, blue sclera
OI types
- mild, blue scl and bone fragile
- lethal, blue scl; severe fragility; no mineralization; skl deformation
- Deform, bl/wh sclera; dentinogenesis imperfecta; fragile; short
- Mild deform, norm scl; dent imp; short; frag-moderate
Ehlers Danlos Syndrome
CT weak - not enough tensile str - hyper skin and joints
Internal complications - ruptured colon, large arts, varricose veins, eccymoses
ED syn types
- coll1/5: joints and skin
- Coll 3: vascular type: arteriol, intestinal, uterine rupture, bruise, thin skin, varricose veins
- Muts lysyl hydroxylase - coll no struc stability. Occular fragility: retinal hemorrhage and detach, corneal rupture, Kyphoscoliosis
- Procoll 1 - coll 1 - joints
Alpart Signal
Common inherited cause of kidney failure
Mut alpha5 chain of type 4 collagen (BL) - Nephrititis and deaf: Haematuria, Proteinuria, HTN
Good Posture syndrome
AutoImmune (20+ males). Antibodies to coll 4 (alpha3 chain) - inflamm destruction of BM in kidney glom and lung alveoli: Haemoptysis and glomeruolomphritis with progressive renal fail
Epidermolysis Bullosa forms
- EBS (EB simplex): mut keratin 5/14
2, Jx’l EB - mut laminin, integrins, hemides - Dys EB - mut coll 7
Butterfly children with extremely fragile skin, friction=blister
Dystrophic EB
Mut coll 7: absence of anchoring filaments, blistering causes syndactyly
FGFR3 Mut: Achondroplasia
Most common dwarfism, 1/100k, <4ft, constituitive expression FGFR3 in chondrocytes - restricts chondrocyte proliferation - excessive bone growth inhib therefore inhibits cartilage growth and coll 2
Stops act of RTK FGFR3 = dwarfism