Browsing by Author "B.S.N. Reddy"
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PublicationArticle Acne cornea or oil acne simulating pityriasis rubra pilaris(1976) R. Singh; B.S.N. Reddy; G. Singh[No abstract available]PublicationArticle An unusual presentation of chronic discoid lupus erythematosus(1976) B.S.N. Reddy; G. Singh[No abstract available]PublicationArticle PublicationArticle Effect of topically applied beclomethasone dipropionate (Propaderm) and hydrocortisone on adrenal function. A preliminary report(1973) Gurmohan Singh; B.S.N. Reddy; Agya Singh KocharBeclomethasone dipropionate (Propaderm), a topical corticosteroid, was compared with hydrocortisone ointment in a double-blind study, to assess its effect on plasma cortisol level. Although potency-wise there was a vast difference between the two steroids (beclomethasone dipropionate being 5000 times as active as hydrocortisone in the McKenzie test), the changes produced in the plasma cortisol levels after the topical application of these two steroids at the end of two weeks were similar. Neither of these steroids produced any appreciable fall in the plasma cortisol level. © 1973.PublicationArticle Leucoderma on remitting lesions of leprosy in reaction. A case report(1977) B.S.N. Reddy; G. Singh[No abstract available]PublicationArticle Peutz-jeghers syndrome(1976) B.S.N. Reddy; Gurmohan Singh; Sushil Chandra; R.P.C. Naik; Rajanikant RaoPeutz-Jeghers syndrome is an uncommon genodermatosis. The clinical and radiological features of Peutz-Jeghers syndrome are described in a 12-year-old male child. The relevant literature is briefly reviewed. © 1976 S. Karger AG, Basel.PublicationArticle Pseudoxanthoma elasticum (Gronblad Strandberg syndrome)(1976) B.S.N. Reddy; G. Singh[No abstract available]PublicationArticle Waardenburg's syndrome with leprosy(1978) B.S.N. Reddy; S. Chandra; P.R. Jha; G. SinghA rare association of Waardenburg's syndrome and tuberculoid leprosy in a 13 year old male patient is described. This is an unrecorded feature in the literature. These two disorders are quite unrelated entities and their occurrence in the same patient is a casual one. All the classical features of Waardenburg's syndrome except deafness were present and the disease manifested as an isolated case in the family. The pertinent literature is briefly reviewed.