Cowden syndrome (CS) is an autosomal dominant condition caused by mutations in the
phosphatase and tensin homolog (PTEN) gene, and is characterized by multiple …

(1) Background: Genodermatoses are a clinically and genetically heterogenous group of
inherited skin disorders. Diagnosing inherited skin diseases is a challenging task due to …

Objective: To study dermoscopic (DS) patterns of various congenital dermatologic conditions
affecting pediatric age group. Background: DS helps to fill gap between histopathology and …

Facial angiofibromas (FAs) are benign skin tumors seen in 80% of patients with tuberous
sclerosis complex (TSC). Full syndrome with skin lesions, mental retardation, and epilepsy …

Dear Editor, Tuberous Sclerosis Complex (TSC) is an autosomal dominant multisystemic
syndrome with a wide range of clinical features. 1–3 The diagnosis is generally easy and is …

A 22-year-old female presented with a 15-year history of multiple asymptomatic papules and
nodules over the face [Figure 1a]. The patient had a history of epilepsy for more than 10 …

For reprints contact: WKHLRPMedknow_reprints@ wolterskluwer. com were considered
[Table 1]. Dermoscopy of facial lesions was performed using 3Gen Dermlite DL4 (CA, USA) …

A punch biopsy from papule revealed nests, cords, and tubules of epithelial cells arranged
in dense fibrous stroma. Ducts were lined by double cuboidal epithelium with a comma‑like …

Kutanöz anjiyofibrom, aynı histolojik özellikleri gösteren ancak farklı klinik bulgulara sahip
bir grup lezyondur ve 4 alt gruba ayrılabilir: fibröz papül, adenoma sebaseum, periungual …

Tuberous sclerosis complex is a rare autosomal dominant neurocutaneous disorder
characterized by the presence of multiple tumors influencing diverse body frameworks …