Reeder and Felson’s Gamuts in Bone, Joint and Spine by Maurice M. Reeder M.D., F.A.C.R. (auth.)

By Maurice M. Reeder M.D., F.A.C.R. (auth.)

All the gamuts bearing on orthopaedics and rheumatology were excerpted from Reeder and Felson's Gamuts in Radiology, the world's top identified, such a lot depended on, and such a lot complete advisor to radiologic differential prognosis. The gamuts were reorganized and renumbered for ease of use. This booklet is principally valuable for citizens in orthopaedics and rheumatology. positive aspects of this derivative contain: - a narrow four x eight" trim measurement for ease of wearing; - a simple to learn single-column structure; - a centred directory of orthopaedic gamuts.

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Additional resources for Reeder and Felson’s Gamuts in Bone, Joint and Spine Radiology: Comprehensive Lists of Roentgen Differential Diagnosis

Example text

Fibrous dysplasia (incl. ) Fracture, traumatic or pathologic (esp. greenstick or healed fracture) Hyperparathyroidism (osteitis fibrosa cystica) Neurofibromatosis (esp. tibia, fibula) Osteogenesis imperfecta Osteomalacia (See B-46) Osteomyelitis, severe (eg, bacterial, tuberculous, smallpox; syphilis-saber shin; yaws-boomerang tibia) Paget's disease Paralysis or restricted movement during growth (eg, poliomyelitis, muscular dystrophy, juvenile rheumatoid arthritis) Physiologic bowing Prenatal bowing of long bones Rickets, all types Tibia vara (Blount's disease) UNCOMMON * I.

5. 6. 7. ) Osteogenesis imperfecta Osteomyelitis (late sequela) Posttraumatic; postoperative (esp. regenerated rib) UNCOMMON 1. 2. 3. 4. Basal cell nevus S. ) Idiopathic Metaphyseal dysplasia (Pyle's disease) Otopalatodigital S. Reference: I. Swischuk LE: Differential Diagnosis in Pediatric Radiology. Bone 33 Gamut 8-10 Gamut B-10 OVERCONSTRICTION OR OVERTUBULATION (NARROW DIAMETAPHYSIS, LONG THIN BONES) COMMON 1. Chronic illness with hypotonia or immobilization 2. Disuse atrophy 3. ) 4. Paralytic disorders (eg, poliomyelitis, cerebral palsy, congenital malformation of brain or spinal cord) UNCOMMON 1.

Dominant form b. recessive forms 5. Oculo-vertebral syndrome (Weyers) **** 6. Osteo-onychodysostosis 7. Cerebro-costo-mandibular syndrome C. Dysostoses with predominant involvement of extremities 1. Acheira 2. Apodia 3. Tetraphoccomelia syndrome (Roberts) (SC pseudothalidomide syndrome) 4. Ectrodactyly a. isolated b. ectrodactyly-ectodermal dysplasia, cleft palate-syndrome c. ectrodactyly with scalp defects 5. Oro-acral syndrome (aglossia syndrome, Hanhart syndrome) 6. Familial radio-ulnar synostosis 7.

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