By Jack J. Kanski MD MS FRCS FRCOphth
One in all ophthalmology's most useful authors, Dr. Jack Kanski, offers a spectrum of scientific symptoms for every during this brand-new diagnostic atlas. Covers almost each ocular illness, with specific concentrate on systemic problems to aid readers diagnose a wealth of ophthalmic stipulations. Discussions emphasize adaptations within the visual appeal and evolution of disorder processes...from the trivial to the serious. Uniquely equipped by way of anatomical sector, this concise, straightforward reference is an exceptional reduction to medical determination making. Over 2,800 full-color photos, many unique to Dr. Kanski's deepest assortment and not earlier than released, depict approximately all affliction stipulations encountered in perform. Illustrations are superior by way of accompanying text―concise, bullet-pointed summaries which are perfect for simple reference. This reference additionally incorporates a CD-ROM containing all the photographs from the textual content, on hand for obtain into digital presentations.
- Serves as an entire diagnostic consultant of ophthalmic disease.
- Features over 2,800 full-color scientific pictures, many unique to Dr. Kanski's inner most collection.
- Includes a CD-ROM containing all the pictures from the text―suitable to obtain for digital presentations.
- Provides concisely written, easy-to-read, templated chapters.
- Offers many angiograms, radiographs, and scans that emphasis pathological processes.
- Organizes subject matters logically―by anatomic region―starting with front of the attention and progressing via to the retina, to make info effortless to find.
- Represents the right consultant for comparability to the whole diversity of stipulations noticeable in perform, or for certification/recertification overview.
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Extra resources for Clinical Diagnosis in Ophthalmology
Forbes and W. F. ) ■ Fig. 133 Diffuse choroidal haemangioma. Klippel–Trenaunay–Weber syndrome ■ Fig. 135 Cutaneous haemangiomas. ■ Fig. 136 Cutaneous haemangiomas, associated with limb hypertrophy. Benign tumours Plexiform neurofibroma ■ Fig. 137 Thickening of the eyelid associated with a mechanical ptosis and a characteristic S-shaped deformity. (Courtesy of K. ) ■ Fig. 138 Eyelid plexiform neurofibroma associated with ipsilateral facial soft tissue hypertrophy. (Courtesy of A. ) Systemic association Neurofibromatosis-1 ■ Fig.
Blepharophimosis syndrome ■ Fig. 216 Bilateral symmetrical ptosis; short horizontal palpebral aperture; telecanthus and epicanthus inversus; lateral ectropion of lower lids; poorly developed nasal bridge and hypoplasia of the superior orbital rims. ■ Fig. 217 The condition is inherited as an autosomal dominant trait. Miscellaneous acquired disorders MISCELLANEOUS ACQUIRED DISORDERS Pseudoptosis A false appearance of ptosis may be caused by the following conditions: Lack of support ■ Fig. 218 Lack of support of the lids by the globe may be due to an orbital volume deficit associated with an artificial eye, microphthalmos, phthisis bulbi or enophthalmos.
249 Subcutaneous calcification and ulceration over bony prominences. ■ Fig. 250 Erythematous (colloidin) papules over finger joints. 63 64 Chapter 1 EYELIDS Scleroderma ■ Fig. 251 Firm, immobile eyelids. Other manifestations ■ Fig. 252 Fixed facial expression with restricted movements of the lips and a ‘beaked’ nose. ■ Fig. 253 Waxy-appearing skin due to tightening and thickening. ■ Fig. 254 Tapering of the fingers with loss of pulps (sclerodactyly). ■ Fig. 255 Subcutaneous calcinosis detectable on plain radiographs.