Limited skeletal survey of a child with with the complaints of growth retardation
Ankylosing Spondylitis
NAIL- PATELLA SYNDROME (Hereditary Osteo Onycho Dysplasia-HOOD)
MYOSITIS OSSIFICANS PROGRESSIVA (Munch Meyer’s disease)
ACROMEGALY
GIGANTISM
SECONDARY HYPERPARATHYROIDISM
Primary Hyperthyroidism as Giantcell tumor
PACHYDERMOPERIOSTOSIS (Primary Hypertrophic Osteoarthropathy)
CRANIOSTENOSIS
CAMPOMELIC DYSPLASIA (CAMTOMELIC DYSPLASIA)
THANATOPHORIC DYSPLASIA
OSTEOPETROSIS (Albers-Schonberg Disease)
OSTEOGENESIS IMPERFECTA
OSTEOPOIKILOSIS
PYLE’S DISEASE (FAMILIAL METAPHYSEAL DYSPLASIA)
MPS IV (MORQUIO-BRAILSFORD SYNDROME) Case 1
MPS IV (Morqio-brailsford Syndrome) Early stage
MPS I (HURLERS SYNDROME)
OSTEOPETROSIS WITH BIRTH TRAUMA
INFANTILE OSTEOPOROSIS
MELORHEOSTOSIS (Leri Disease)
Asphyxiating Thoracic Dystrophy (Jeune Syndrome)
ACHONDROGENESIS
Osteo poikilosis with Osteopathia striata (Overlapping syndromes)
OTEOPATHIA STRIATA ( VOORHOEVES DISEASE)
CHONDR ECTODERMAL DYSPLASIA (Ellis-Vancreveld syndrome)
Achondroplasia Adult
Achondroplasia Child
METAPHYSEAL CHONDRODYSPLASIA (Schmidt Type)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA(X0a-Linked spondyloepiphyseal dysplasia)
OSTEOPETROSIS (Tarda) WITH FRACTURE
CLEIDO CRANIAL DYSOSTOSIS
Spondyloepiphyseal Dysplasia Congenita
Dysplasia Epiphysealis Punctata – Lethal
Multiple Epiphyseal Dysplasia
Dysplasia Epiphysealis Punctata
