Results 91 to 100 of about 10,708 (219)

Safety and efficacy of travoprost solution for the treatment of elevated intraocular pressure [PDF]

open access: yes, 2015
Travoprost is a prostaglandin analogue widely used for reducing intraocular pressure (IOP) in patients affected with glaucoma and ocular hypertension. It exerts its ocular hypotensive effect through the prostaglandin FP receptors, located in the ciliary ...
Centofanti, Marco   +5 more
core   +2 more sources

Frequency of Hirsutism among females students in Babol University of Medical Sciences, 1999

open access: yesMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2002
Background and Objective: The objective of this study was determination of the frequency of hirsutism among female students and its relationship with menstrual abnormality, acne, androgenetic alopecia, hypertrichosis and familial history of hirsutism ...
S Tirgar Tabari   +3 more
doaj  

Solitary Asymptomatic Plaque Over the Knee of 1-year-old Girl

open access: yesIndian Journal of Paediatric Dermatology
Eccrine angiomatous hamartoma is a rare benign malformation of eccrine and vascular structures. It often presents as a nodule or a plaque usually on the lower extremities. It may present at birth or in the early childhood.
Divya Jaju   +2 more
doaj   +1 more source

CLINICO-HORMONAL VARIANTS OF THE SYNDROME OF HYPERANDROGENIA

open access: yesŽurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, 2018
Endocrine diseases accompanied by hyperandrogenia and disorder of the reproductive function of the body occur in clinical practice. This article reviews the main genetic and hormonal changes, as well as clinical manifestations of the syndrome of ...
Nikonova L. V.   +3 more
doaj   +1 more source

Hypertrichosis: the possible side effect of cyclosporin in an infant with hemophagocyticlymphohistiocytosis receiving HLH-2004 chemotherapy protocol

open access: yesTurkish Journal of Hematology, 2009
Hemophagocyticlymphohistiocytosis is a life-threatening condition of severe hyperinflammation that results from an uncontrolled proliferation of activated lymphocytes and histiocytes secreting high amounts of inflammatory cytokines.
Sinem Akgül   +4 more
doaj  

H syndrome - A case report

open access: yesIndian Dermatology Online Journal, 2019
This case report describes a case of H syndrome with characteristic cutaneous hyperpigmentation, hypertrichosis, sclerodermatous thickening, and multisystem involvement such as hearing loss and heart anomaly in an Indian patient.
Patrick Yesudian   +3 more
doaj   +1 more source

Dysmorphophobia in a Diastrophic Dwarf: A Psychiatry-Dermatology Liaison Approach [PDF]

open access: yes, 2011
This is a case study of a 30-year-old male diastrophic dwarf who complained of hypertrichosis on his back and nose of 3 years duration. He had no previous psychiatric history, and although the distortion he described on his back was not apparent to ...
Kushon, MD, Donald J.
core   +1 more source

Hipertricosis adquirida y localizada en fascitis eosinofílica [PDF]

open access: yes, 2013
La fascitis eosinofílica, se caracteriza por cambios cutáneos símil- esclerodermia y eosinofília periférica. Describimos un paciente de 54 años, de sexo masculino con diagnóstico de fascitis eosinofílica y seguimiento de 44 meses. Presentaba tumefacción,
Abaca, Héctor E.   +1 more
core  

Topical latanoprost does not cause macular thickening after uncomplicated cataract surgery. [PDF]

open access: yes, 2012
PurposeTo explore changes in central macular thickness (CMT) after a two-month period of glaucoma therapy with topical latanoprost after uneventful phacoemulsification.MethodsForty-one eyes of 31 patients with primary open angle or pseudoexfoliative ...
Amini, Heydar   +7 more
core   +1 more source

Unmasking Günther Disease: A Rare Case of Congenital Erythropoietic Porphyria in a Young Boy

open access: yesIndian Journal of Paediatric Dermatology
Congenital erythropoietic porphyria (CEP), or Günther disease, is a rare autosomal recessive disorder marked by severe photosensitivity, hemolytic anemia, and skin fragility due to uroporphyrinogen III synthase deficiency. We report a 6-year-old boy with
Biju Vasudevan   +3 more
doaj   +1 more source

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