poikiloderma

Between 3 to 6 months of age, the affected carrier develops poikiloderma on the cheeks.

Other names for the condition include prereticulotic poikiloderma and atrophic parapsoriasis.

Rothmund-Thomson syndrome, also known as poikiloderma congenitale, is a heritable disorder characterized by chromosomal instability.

In modern consideration and usage, the solitary term "poikiloderma" has also come to represent all three elements of PVA.

Among them, xeroderma pigmentosum and Rothmund-Thomson syndrome (poikiloderma congenita) are thought to be the most prominent.

Poikiloderma of Civatte is a cutaneous condition and refers to reticulated red to red-brown patches with telangiectasias.

The exact cause of poikiloderma is unknown; however, extended sun exposure, namely the ultraviolet light emitted by the sun, is the primary factor.

Poikiloderma is a skin condition that consists of areas of increased and decreased pigmentation, prominent blood vessels, and thinning of the skin.

Albeit difficult, treatment of poikiloderma involves the delivery of multiple wavelengths of intense pulsed light (IPL) to the affected area.

Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood.

Haneke E, Gutschmidt E: Premature multiple Bowen's disease in poikiloderma congenitale with warty hyperkeratoses.

PVA can occur in either the large plaque or retiform stage, but it can only be considered PVA when its three constituents (poikiloderma, telangiectasia, atrophy) are present.

Usage of the entire term "poikiloderma vasculare atrophicans" may also be reserved to indicate it as the primary condition affecting the skin in cases where the disorder associated with it is secondary.

Large-plaque parapsoriasis is a common associate of retiform parapsoriasis, can be accompanied by poikiloderma vasculare atrophicans, and can in rare occasions be a precursor to cutaneous T-cell lymphoma.

When skin diseases and disorders or skin conditions described as dermatoses contain the term poikiloderma in their assessment or diagnosis (such as with Bloom syndrome), this can sometimes be an erroneous usage of the term.

Rothmund-Thomson syndrome, also known as poikiloderma congenitale, is characterized by premature aging, skin and skeletal abnormalities, rash, poikiloderma, juvenile cataracts, and a predisposition to cancers such as osteosarcomas.

Rothmund-Thomson syndrome (RTS), also known as poikiloderma atrophicans with cataract or poikiloderma congenitale, is a rare autosomal recessive skin condition originally described by August von Rothmund (1830-1906) in 1868.

Rothmund-Thomson syndrome, or poikiloderma congenitale, is a rare disorder, generally attributed to mutations of the RECQL4 helicase gene on 8q24 with features that include photosensitivity and poikilodermatous skin changes, etc., and has been reported in one celiac patient.

Poikiloderma Congenitale Poikiloderma Atrophicans and Cataract RTS None Rothmund-Thomson syndrome (RTS) is a rare genetic disorder that can affect many parts of the body.

The ultrapigmented condition in which dilated blood vessels and brown spots proliferate on the neck and chest goes by the clinical name of poikiloderma; the best means of avoiding it are to stay out of the sun and to use prescription-strength products on the area, ones that contain retinols and hydroquinone.