Volume 27 (2024)
Volume 26 (2023)
Volume 25 (2022)
Volume 24 (2021)
Volume 23 (2020)
Volume 22 (2019)
Volume 21 (2018)
Volume 20 (2017)
Volume 19 (2016)
Volume 18 (2015)
Volume 17 (2014)
Volume 16 (2013)
Volume 15 (2012)
Volume 14 (2011)
Volume 13 (2010)
Volume 12 (2009)
Volume 11 (2008)
Volume 10 (2007)
Volume 9 (2006)
Volume 8 (2005)
Volume 7 (2004)
Volume 6 (2002)
Volume 5 (2002)
Volume 4 (2000)
Volume 3 (1999)
Volume 2 (1998)
Volume 1 (1997)
Acute blue finger syndrome: a case report

Saurabh Sharma; Vinay Kajal; Parwaaz Matharoo; Roopam Bassi

Volume 25, Issue 1 , March 2022, , Pages 73-75

https://doi.org/10.22034/ijd.2020.230813.1094

Abstract
  Acute blue finger syndrome is a rare benign condition with an unknown etiology. It predominantly affects middle-agedfemales and may be associated with pain, itching, or a burning sensation. The bluish discoloration is usually idiopathic, and it is necessary to rule out other causes of blue fingers. The ...  Read More

An uncommon presentation of pachyonychia congenital

Amirhushang Ehsani; Fatemeh Moeineddin; Ahmadreza Rajaee

Volume 10, Suppl.2 , 2007, , Pages 8-8

Abstract
  A 10-month-old female presented with severe progressive wedge-shaped thickening and discoloration of all twenty nails. Further evaluations revealed palmoplantar keratoderma along with recurrent acral blisters causing residual crusted ulcers which were present during the past six months. Other findings ...  Read More

An Iranian family with cutis laxa and classic Ehlers-Danlos syndrome

Vahid Mashayekhi Guyunlou; Nasser Tayyebi Meybodi; Zari Javidi; Mahmoud Farhoudi; Yalda Nahidi

Volume 9, suppl.1 , 2006, , Pages 10-10

Abstract
  Ehlers-Danlos syndrome (EDS) is a heterogenous group of inherited disorders of connective tissue characterized by fragility of the skin and blood vessels, hyperextensibility of the skin and joint hypermobility. Cutis laxa is characteized clinically by lax, pendulous skin and histologically by loss of ...  Read More

Goltz syndrome: A case report

Pouran Layegh; Parisa Emamgholitabar Malekshah; Seyyed Reza Mousavi

Volume 9, suppl.1 , 2006, , Pages 11-11

Abstract
  Goltz syndrome / Focal Dermal Hypoplasia (FDH) is a rare syndrome resulting from developmental defects in tissues with mesodermal origin such as eye, skin, mouth, muscoloskeletal, and central nervous system. We report a 13-year-old girl with FDH who had several features of skin, eye, and mouth involvement. ...  Read More

A case report of Churg-Strauss syndrome in peripartum period

H Poor Moghim; M Rezaei Salim

Volume 8, suppl , 2004, , Pages 53-58

Abstract
  Allergic granulomatous angiitis (Churg-Strauss syndrome) is a variant of systemic vasculitis characterized by pulmonary and systemic small vessel vasculitis, extra-vascular granulomas and eosinophilia. Clinical features include presence of asthma and/or allergic rhinitis with constitutional symptoms ...  Read More