Document Type : Case Report
Authors
- Mohammadi Saman
- Khalili Maryam
- Fadai Fahameh
- Badakhsh Hoda
- Farajzadeh Saeedeh
- Mohebbi Azadeh
- Aflatoonian Mahin
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
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