The topic Fischer-Jacobsen-Clouston Syndrome you are seeking is a synonym, or alternative name, or is closely related to the medical condition Hidrotic Ectodermal Dysplasia 2.

Quick Summary:

• Hidrotic Ectodermal Dysplasia 2 (HED2) may be described as an uncommon form of hereditary diffuse palmoplantar keratoderma that is transmitted in an autosomal dominant manner. The condition manifests during childhood and is characterized by a triad of features that include palmoplantar keratoderma, nail abnormalities, and partial or complete hair loss
• Hereditary diffuse palmoplantar keratoderma is a type of palmoplantar keratoderma (PPK) caused by genetic mutations. PPK is a benign skin condition, wherein there is thickening of skin (keratoderma) of the palms and/or soles. PPK is considered to be a pattern of skin findings and not a condition in itself. The abnormal skin thickening can be focal (localized), widespread (diffused), or punctate type (appearing as tiny bumps)
• The signs and symptoms of Hidrotic Ectodermal Dysplasia 2 are progressive; however, an involvement of other body systems or organs is not noted. The treatment for the condition involves the use of moisturizers, hair care products, skin softeners, and systemic medications. The prognosis is determined on a case-by-case basis, but HED2 is a lifelong condition

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