Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy. Poikiloderma of Civatte is...

Poikiloderma vasculare atrophicans (PVA), is a cutaneous condition (skin disease) characterized by hypo- or hyperpigmentation (diminished or heightened...

has been implicated in the syndrome. Sun-sensitive rash with prominent poikiloderma and telangiectasias Juvenile cataracts Saddle nose Congenital bone defects...

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

Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary") is a type of epidermolysis bullosa, a rare congenital disease...

Incontinentia pigmenti (IP) is a rare X-linked dominant genetic disorder that affects the skin, hair, teeth, nails and central nervous system. It is named...

hours) Granuloma Livedo Purpura Erythema (redness) Horn (a cell type) Poikiloderma Hyperkeratosis Parakeratosis Hypergranulosis Acanthosis Papillomatosis...

Side effects may be mild, such as itchiness, folliculitis, sunburn, poikiloderma, and a theoretical risk of nonmelanoma cancer or melanoma has been suggested...

poikiloderma, bullous acrokeratotic poikiloderma of Kindler and Weary, congenital poikiloderma with blisters and keratoses, congenital poikiloderma with...

alignment, a thin-film-transistor liquid-crystal display technology Poikiloderma vasculare atrophicans, a skin disease Polyvinyl acetate, an adhesive...

right third intercostal nerve through its anterior cutaneous branch. Poikiloderma of Civatte, a condition of dilated blood vessels and red to red-brown...

including photodamage induced dyspigmentation and vascular changes, poikiloderma of Civatte, rosacea, acne vulgaris, sebaceous gland hyperplasia, broken...

perstans Lichen planus pigmentosus Café au lait spot Poikiloderma (Poikiloderma of Civatte Poikiloderma vasculare atrophicans) Riehl melanosis Linear Incontinentia...

phototoxicity, nevus of Ota, café au lait macules, seborrheic keratosis, Poikiloderma of Civatte, acquired bilateral nevus of ota-like macules (Hori's nevus)...

fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis is a rare genetic syndrome characterised by poikiloderma, tendon contractures...

Ectodermal dysplasias Clouston's hidrotic ectodermal dysplasia Acrokeratotic poikiloderma Dermatopathic pigmentosa reticularis Syndromic keratodermas Vohwinkel...

retardation Poikiloderma congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Kindler Poikiloderma of Rothmund–Thomson...

Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive gait disorder. The disease presents with progressive...

scapular anomalies Pierre Robin syndrome-faciodigital anomaly syndrome Poikiloderma with neutropenia Polymicrogyria with or without vascular-type Ehlers-Danlos...

Naegeli–Franceschetti–Jadassohn syndrome (NFJS), also known as chromatophore nevus of Naegeli and Naegeli syndrome, is a rare autosomal dominant form of...

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

a common associate of retiform parapsoriasis, can be accompanied by poikiloderma vasculare atrophicans, and can in rare occasions be a precursor to cutaneous...

lichenoides et varioliformis acuta Lymphomatoid papulosis Mycosis Fungoides Poikiloderma vasculare atrophicans List of cutaneous conditions Sehgal VN, Srivastava...

Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum/Pseudo-ainhum...

syndrome, also known as poikiloderma congenitale, is characterized by premature aging, skin and skeletal abnormalities, rash, poikiloderma, juvenile cataracts...

Spastic paraplegia nephritis deafness Spastic paraplegia neuropathy poikiloderma Spastic paraplegia type 1, X-linked Spastic paraplegia type 2, X-linked...

characteristics sometimes associated with this disorder are growth retardation and poikiloderma. Although the presentation of BGS may differ between individuals, these...

pseudoobstruction patent ductus Nathalie syndrome Native American myopathy Navajo poikiloderma Naxos disease Necrotizing encephalopathy, infantile subacute Necrotizing...

hands and feet, and typical facial changes.: 576  Hereditary sclerosing poikiloderma Skin lesion "Mandibuloacral dysplasia". Genetic and Rare Diseases. NIH...

Gannavarapu A, Clericuzio CL, et al. (2004). "Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients". Am. J. Med. Genet...