@article { author = {Saman, Mohammadi and Maryam, Khalili and Fahameh, Fadai and Hoda, Badakhsh and Saeedeh, Farajzadeh and Azadeh, Mohebbi and Mahin, Aflatoonian}, title = {Focal dermal hypoplasia (Goltz) syndrome with multiple family member involvement: A case report}, journal = {Iranian Journal of Dermatology}, volume = {20}, number = {4}, pages = {131-134}, year = {2017}, publisher = {Iranian Society of Dermatology}, issn = {2717-0721}, eissn = {2717-0721}, doi = {}, abstract = {Goltz syndrome or focal dermal hypoplasia is a rare syndrome with mesoectodermal hypoplasia. This syndrome is an X-linked dominant disorder with involvement of the cutaneous, ocular, dental and skeletal systems. The most significant feature of this disease is connective tissue dysplasia. Here, we report a 30-year old woman who presented with congenital unilateral linear atrophic areas on her trunk, back, and upper and lower extremit}, keywords = {Goltz syndrome,clinodactyly,Hypoplasia}, url = {https://www.iranjd.ir/article_98334.html}, eprint = {https://www.iranjd.ir/article_98334_0667fb5ef20ab85a29111e5d9ecd9c37.pdf} }