Multiple fractures

A skull fracture is a break in one or more of the eight bones that form the cranial portion of the skull, usually occurring as a result of blunt force trauma. If the force of the impact is excessive, the bone may fracture at or near the site of the impact and cause damage to the underlying structures within the skull such as the membranes, blood vessels, and brain. [Source: Wikipedia ]

May Be Caused by
Achondrogenesis type 1
Aluminum-induced bone disease
Angiomatosis
Antley-Bixler syndrome
Arthrogryposis
Aspartylglucosaminuria
Battered child syndrome
Campomelic dysplasia
Carcinomatosis
Cleidocranial dysostosis
Congenital insensitivity to pain
Congenital syphilis
Cushing syndrome
Cystic type lymphangiomatosis
Cystinosis
Diffuse osteomyelitis
Dysosteosclerosis
Electroconvulsive therapy
Enchondromatosis
Fibrogenesis imperfecta ossium
Gaucher disease
Gerodermia osteodysplastica
Glycogen storage disease type 1
GM1 gangliosidosis
Hemangiomatosis
Homocystinuria
Hydatid disease
Hyperphosphatasia
Hypophosphatasia
Juvenile idiopathic osteoporosis
Langerhans cell histiocytosis
Lethal micromelic-facial bones sclerosis dysplasia
Leukemia
Lowe syndrome
Maffucci syndrome
Membranous lipodystrophy
Menkes disease
Metaphyseal chondrodysplasia Jansen type
Metastasis
Milkman syndrome
Mucolipidosis type 2
Multiple myeloma
Myelomatosis
Niemann-Pick disease
Nutritional copper deficiency
Osteitis fibrosa cystica
Osteogenesis imperfecta
Osteomalacia
Osteopetrosis
Osteoporosis
Oxalosis
Paget disease of bone
Polyostotic fibrous dysplasia
Primary anemia
Primary hyperparathyroidism
Progeria
Pyknodysostosis
Pyle dysplasia
Renal osteodystrophy
Renal tubular acidosis
Riley-Day syndrome
Scurvy
Secondary hyperparathyroidism
Seizure
Severe rickets
Spondylometaphyseal dysplasia corner fracture type
Steroid medication
Stiff-man syndrome
Tetanus
Thalassemia
Thevenard syndrome
Trauma
Trichorhinophalangeal dysplasia type 2
Werdnig-Hoffmann disease
Wilson disease
Achondrogenesis type 1
Aluminum-induced bone disease
Angiomatosis
Antley-Bixler syndrome
Arthrogryposis
Aspartylglucosaminuria
Battered child syndrome
Campomelic dysplasia
Carcinomatosis
Cleidocranial dysostosis
Congenital insensitivity to pain
Congenital syphilis
Cushing syndrome
Cystic type lymphangiomatosis
Cystinosis
Diffuse osteomyelitis
Dysosteosclerosis
Electroconvulsive therapy
Enchondromatosis
Fibrogenesis imperfecta ossium
Gaucher disease
Gerodermia osteodysplastica
Glycogen storage disease type 1
GM1 gangliosidosis
Hemangiomatosis
Homocystinuria
Hydatid disease
Hyperphosphatasia
Hypophosphatasia
Juvenile idiopathic osteoporosis
Langerhans cell histiocytosis
Lethal micromelic-facial bones sclerosis dysplasia
Leukemia
Lowe syndrome
Maffucci syndrome
Membranous lipodystrophy
Menkes disease
Metaphyseal chondrodysplasia Jansen type
Metastasis
Milkman syndrome
Mucolipidosis type 2
Multiple myeloma
Myelomatosis
Niemann-Pick disease
Nutritional copper deficiency
Osteitis fibrosa cystica
Osteogenesis imperfecta
Osteomalacia
Osteopetrosis
Osteoporosis
Oxalosis
Paget disease of bone
Polyostotic fibrous dysplasia
Primary anemia
Primary hyperparathyroidism
Progeria
Pyknodysostosis
Pyle dysplasia
Renal osteodystrophy
Renal tubular acidosis
Riley-Day syndrome
Scurvy
Secondary hyperparathyroidism
Seizure
Severe rickets
Spondylometaphyseal dysplasia corner fracture type
Steroid medication
Stiff-man syndrome
Tetanus
Thalassemia
Thevenard syndrome
Trauma
Trichorhinophalangeal dysplasia type 2
Werdnig-Hoffmann disease
Wilson disease