منابع مشابه
Ocular findings in haemochromatosis.
HAEMOCHROMATOSIS is a rare condition, the chief clinical features of which are pigmentation of the skin, cirrhosis of the liver, diabetes mellitus, and hypogonadism. The opportunity of examining the eyes of five patients in whom the diagnosis had been confirmed by liver biopsy arose through the kindness of my colleague, Dr. N. F. Coghill, who is incorporating the clinical and pathological inves...
متن کاملDeposition of melanin and iron in ocular structures in haemochromatosis
Cutaneous pigmentation is a well-recognized feature of idiopathic haemochromatosis and, in various series, has been recorded in up to 8o per cent. of patients (Finch and Finch, I955). In the world literature there are occasional reports of pigmentation in the gums (Saundby, I890), buccal mucous membranes (Richardiere, I895), lips (Parker, I903), and tongue (Hess and Zurhelle, I905), and Maddox ...
متن کاملDeposition of melanin and iron in ocular structures in haemochromatosis.
Cutaneous pigmentation is a well-recognized feature of idiopathic haemochromatosis and, in various series, has been recorded in up to 8o per cent. of patients (Finch and Finch, I955). In the world literature there are occasional reports of pigmentation in the gums (Saundby, I890), buccal mucous membranes (Richardiere, I895), lips (Parker, I903), and tongue (Hess and Zurhelle, I905), and Maddox ...
متن کاملUltrasonographic findings of some ocular structures in Caspian miniature horse
Ultrasonography is a relatively easy, safe and non-invasive examination method which can be used in diagnosis of ocular disorders as complementary to routine ophthalmic examinations. As there has been no collated study undertaken on the normal measurements of ocular structures in Caspian miniature horse, obtaining these measurements could be a benchmark to diagnose some of the diseases and eye ...
متن کاملOcular findings in muscular dystrophies
Muscular dystrophies are a heterogeneous class of inherited disorders presenting with different clinical, genetic, and biochemical features. Muscular dystrophies include Duchennemuscular dystrophy (DMD) and Becker muscular dystrophy (BMD) myotonic dystrophy (DM), oculopharyngeal muscular dystrophy (OPMD), facioscapulohumeral muscular dystrophy (FSHD), limb-girdle muscular dystrophy (LGMD), dist...
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ژورنال
عنوان ژورنال: British Journal of Ophthalmology
سال: 1953
ISSN: 0007-1161
DOI: 10.1136/bjo.37.4.242