Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy. Poikiloderma of Civatte is...
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Poikiloderma of Civatte is a cutaneous condition and refers to reticulated red to red-brown skin patches with telangiectasias. It is identifiable as a...
2 KB (154 words) - 22:48, 4 November 2023
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) - 19:56, 23 August 2024
Kindler syndrome (redirect from Acrokeratotic poikiloderma)
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary") is a rare congenital disease of the skin caused by a mutation...
6 KB (436 words) - 14:05, 19 September 2024
Poikiloderma vasculare atrophicans (PVA), is a cutaneous condition (skin disease) characterized by hypo- or hyperpigmentation (diminished or heightened...
13 KB (1,357 words) - 15:11, 7 August 2022
Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood...
2 KB (76 words) - 00:48, 6 May 2024
fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis is a rare genetic syndrome characterised by poikiloderma, tendon contractures...
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Ectodermal dysplasias Clouston's hidrotic ectodermal dysplasia Acrokeratotic poikiloderma Dermatopathic pigmentosa reticularis Syndromic keratodermas Vohwinkel...
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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...
24 KB (2,733 words) - 16:35, 9 March 2024
perstans Lichen planus pigmentosus Café au lait spot Poikiloderma (Poikiloderma of Civatte Poikiloderma vasculare atrophicans) Riehl melanosis Linear Incontinentia...
39 KB (3,838 words) - 16:01, 26 September 2024
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 (447 words) - 15:04, 27 October 2023
retardation Poikiloderma congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Kindler Poikiloderma of Rothmund–Thomson...
24 KB (1,908 words) - 03:34, 11 January 2024
alignment, a thin-film-transistor liquid-crystal display technology Poikiloderma vasculare atrophicans, a skin disease Polyvinyl acetate, an adhesive...
1 KB (165 words) - 09:29, 25 July 2023
poikiloderma, bullous acrokeratotic poikiloderma of Kindler and Weary, congenital poikiloderma with blisters and keratoses, congenital poikiloderma with...
198 KB (17,960 words) - 17:11, 27 September 2024
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 (13,059 words) - 13:20, 22 September 2024
scapular anomalies Pierre Robin syndrome-faciodigital anomaly syndrome Poikiloderma with neutropenia Polymicrogyria with or without vascular-type Ehlers-Danlos...
14 KB (1,343 words) - 13:07, 21 September 2024
hours) Granuloma Livedo Purpura Erythema (redness) Horn (a cell type) Poikiloderma Hyperkeratosis Parakeratosis Hypergranulosis Acanthosis Papillomatosis...
28 KB (2,681 words) - 10:31, 21 March 2024
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...
11 KB (1,078 words) - 17:37, 23 July 2024
phototoxicity, nevus of Ota, café au lait macules, seborrheic keratosis, Poikiloderma of Civatte, acquired bilateral nevus of ota-like macules (Hori's nevus)...
17 KB (1,911 words) - 20:07, 19 August 2024
including photodamage induced dyspigmentation and vascular changes, poikiloderma of Civatte, rosacea, acne vulgaris, sebaceous gland hyperplasia, broken...
18 KB (2,106 words) - 12:33, 2 July 2024
Spastic paraplegia nephritis deafness Spastic paraplegia neuropathy poikiloderma Spastic paraplegia type 1, X-linked Spastic paraplegia type 2, X-linked...
23 KB (1,933 words) - 06:25, 11 July 2024
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) - 19:00, 17 April 2024
hands and feet, and typical facial changes.: 576 Hereditary sclerosing poikiloderma Skin lesion "Mandibuloacral dysplasia". Genetic and Rare Diseases. NIH...
3 KB (182 words) - 23:57, 6 May 2024
syndrome, also known as poikiloderma congenitale, is characterized by premature aging, skin and skeletal abnormalities, rash, poikiloderma, juvenile cataracts...
56 KB (6,916 words) - 17:01, 27 August 2024
lichenoides et varioliformis acuta Lymphomatoid papulosis Mycosis Fungoides Poikiloderma vasculare atrophicans List of cutaneous conditions Sehgal VN, Srivastava...
3 KB (196 words) - 23:51, 1 July 2023
Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum/Pseudo-ainhum...
6 KB (673 words) - 12:15, 11 April 2024
characteristics sometimes associated with this disorder are growth retardation and poikiloderma. Although the presentation of BGS may differ between individuals, these...
9 KB (912 words) - 19:52, 23 August 2024
characterized by deep furrowing of the skin. List of cutaneous conditions Poikiloderma of Civatte Solar elastosis Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo...
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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) - 00:22, 25 November 2023
pseudoobstruction patent ductus Nathalie syndrome Native American myopathy Navajo poikiloderma Naxos disease Necrotizing encephalopathy, infantile subacute Necrotizing...
8 KB (654 words) - 16:03, 15 March 2024