Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy. Poikiloderma of Civatte is...
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Poikiloderma vasculare atrophicans (PVA), is a cutaneous condition (skin disease) characterized by hypo- or hyperpigmentation (diminished or heightened...
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Rothmund–Thomson syndrome (redirect from Poikiloderma congenitale)
has been implicated in the syndrome. Sun-sensitive rash with prominent poikiloderma and telangiectasias Juvenile cataracts Saddle nose Congenital bone defects...
10 KB (914 words) - 15:27, 23 October 2024
Poikiloderma of Civatte is a cutaneous condition and refers to reticulated red to red-brown skin patches with telangiectasias. It is identifiable as a...
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Kindler syndrome (redirect from Acrokeratotic poikiloderma)
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary") is a type of epidermolysis bullosa, a rare congenital disease...
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Side effects may be mild, such as itchiness, folliculitis, sunburn, poikiloderma, and a theoretical risk of nonmelanoma cancer or melanoma has been suggested...
116 KB (12,948 words) - 16:37, 19 July 2025
Incontinentia pigmenti (redirect from Poikiloderma with incontinentia pigmenti)
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...
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hours) Granuloma Livedo Purpura Erythema (redness) Horn (a cell type) Poikiloderma Hyperkeratosis Parakeratosis Hypergranulosis Acanthosis Papillomatosis...
28 KB (2,683 words) - 06:07, 6 February 2025
poikiloderma, bullous acrokeratotic poikiloderma of Kindler and Weary, congenital poikiloderma with blisters and keratoses, congenital poikiloderma with...
198 KB (17,982 words) - 07:12, 15 July 2025
perstans Lichen planus pigmentosus Café au lait spot Poikiloderma (Poikiloderma of Civatte Poikiloderma vasculare atrophicans) Riehl melanosis Linear Incontinentia...
42 KB (4,186 words) - 15:30, 17 July 2025
alignment, a thin-film-transistor liquid-crystal display technology Poikiloderma vasculare atrophicans, a skin disease Polyvinyl acetate, an adhesive...
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retardation Poikiloderma congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Kindler Poikiloderma of Rothmund–Thomson...
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phototoxicity, nevus of Ota, café au lait macules, seborrheic keratosis, Poikiloderma of Civatte, acquired bilateral nevus of ota-like macules (Hori's nevus)...
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Intermammary cleft (section Poikiloderma of Civatte)
right third intercostal nerve through its anterior cutaneous branch. Poikiloderma of Civatte, a condition of dilated blood vessels and red to red-brown...
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including photodamage induced dyspigmentation and vascular changes, poikiloderma of Civatte, rosacea, acne vulgaris, sebaceous gland hyperplasia, broken...
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Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood...
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Ectodermal dysplasias Clouston's hidrotic ectodermal dysplasia Acrokeratotic poikiloderma Dermatopathic pigmentosa reticularis Syndromic keratodermas Vohwinkel...
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Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive gait disorder. The disease presents with progressive...
36 KB (3,347 words) - 17:31, 16 July 2025
scapular anomalies Pierre Robin syndrome-faciodigital anomaly syndrome Poikiloderma with neutropenia Polymicrogyria with or without vascular-type Ehlers-Danlos...
15 KB (1,454 words) - 17:26, 17 July 2025
fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis is a rare genetic syndrome characterised by poikiloderma, tendon contractures...
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Naegeli–Franceschetti–Jadassohn syndrome (redirect from Congenital poikiloderma with bulla formation)
Naegeli–Franceschetti–Jadassohn syndrome (NFJS), also known as chromatophore nevus of Naegeli and Naegeli syndrome, is a rare autosomal dominant form of...
5 KB (445 words) - 15:04, 27 October 2023
Spastic paraplegia nephritis deafness Spastic paraplegia neuropathy poikiloderma Spastic paraplegia type 1, X-linked Spastic paraplegia type 2, X-linked...
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Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum/Pseudo-ainhum...
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lichenoides et varioliformis acuta Lymphomatoid papulosis Mycosis Fungoides Poikiloderma vasculare atrophicans List of cutaneous conditions Sehgal VN, Srivastava...
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syndrome, also known as poikiloderma congenitale, is characterized by premature aging, skin and skeletal abnormalities, rash, poikiloderma, juvenile cataracts...
55 KB (6,753 words) - 22:59, 12 July 2025
characteristics sometimes associated with this disorder are growth retardation and poikiloderma. Although the presentation of BGS may differ between individuals, these...
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pseudoobstruction patent ductus Nathalie syndrome Native American myopathy Navajo poikiloderma Naxos disease Necrotizing encephalopathy, infantile subacute Necrotizing...
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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...
10 KB (1,245 words) - 18:08, 17 July 2025
hands and feet, and typical facial changes.: 576 Hereditary sclerosing poikiloderma Skin lesion "Mandibuloacral dysplasia". Genetic and Rare Diseases. NIH...
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which occur in >75% of patients, include erythroderma, pruritus, eczema, poikiloderma, urticarial, and episodic angioedema. The symptom of episodic angioedema...
20 KB (2,341 words) - 03:41, 9 July 2025