PACHYDERMOPERIOSTOSIS (Primary Hypertrophic Osteoarthropathy)

Young male patient with hyperhydrosis and coarse features of face

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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