-
popliteal pteryg Spondylometaphyseal dysplasia, 'corner fracture' t
Spondylometaphyseal dysplasia,
Schmidt type
Spondylometaphyseal dysplasia, Sedaghatian...
- Saethre-Chotzen
syndrome Spondyloenchondrodysplasia with
immune dysregulation Spondylometaphyseal dysplasia,
Sedaghatian type
Summitt syndrome Teebi-Shaltout syndrome...
-
Spondyloepimetaphyseal dysplasia is a
genetic condition affecting the bones.
Types include:
Spondyloepimetaphyseal dysplasia,
Strudwick type Spondyloepiphyseal...
-
Spondylometaphyseal dysplasia, East-African type is a rare
genetic disorder which is
characterized by
skeletal abnormalities involving the
vertebrae and...
-
Spondyloepimetaphyseal dysplasia-short limb-abnormal
calcification syndrome Spondylometaphyseal dysplasia with
corneal dystrophy Tetralogy of
Fallot Thyroid hormone...
-
Spondylometaphyseal dysplasia with cone-rod
dystrophy is a rare
genetic disorder characterized by
spondylometaphyseal dysplasia (which
consists of platyspondyly...
- S2CIDÂ 31820771. Frydman, M., Preminger-Shapiro, R., Bar-Ziv, J.
Spondylometaphyseal dysplasia with 'enchondromatous-like' changes--a
distinctive type...
-
Autosomal recessive faciodigitogenital syndrome Autosomal recessive spondylometaphyseal dysplasia,
Megarbane type Bartsocas-Papas
syndrome 1 Bilateral...
- peroxides,
resulting in
ferroptotic cell death.
Mutations in GPX4
cause spondylometaphyseal dysplasia. In
vitro studies suggest that GPX4
protects cells against...
- 6--phosphate
receptor recognition defect (1984),
Algerian type of
spondylometaphyseal dysplasia (1988),
Kuwaiti type of
cardioskeletalsyndrome (1990),...
