Hereditary sclerosing poikiloderma with tendon and pulmonary involvement (Q101666): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 18:30, 16 August 2026
In this condition, reported from South Africa, hereditary sclerosing poikiloderma is associated with pulmonary disease which is potentially lethal in adulthood. Skin manifestations which facilitate diagnosis include facial telangiectasia, mottled hypo- and hyperpigmentation, papules and epidermal atrophy. The scalp, facial and body hair are fine and scanty. The tendon contractures lead to progressive digital flexion deformities and abnormalities of the ankles and feet, with disturbance of gait. Pulmonary involvement manifests as progressive dyspnoea. Pedigree data are compatible with an autosomal dominant mode of transmission (PMID: 17034542).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1585528459 |
||
| English | Hereditary sclerosing poikiloderma with tendon and pulmonary involvement |
In this condition, reported from South Africa, hereditary sclerosing poikiloderma is associated with pulmonary disease which is potentially lethal in adulthood. Skin manifestations which facilitate diagnosis include facial telangiectasia, mottled hypo- and hyperpigmentation, papules and epidermal atrophy. The scalp, facial and body hair are fine and scanty. The tendon contractures lead to progressive digital flexion deformities and abnormalities of the ankles and feet, with disturbance of gait. Pulmonary involvement manifests as progressive dyspnoea. Pedigree data are compatible with an autosomal dominant mode of transmission (PMID: 17034542). |
Statements
CID11:ID_1585528459
0 references
dki-india-ID_1585528459
0 references
Concluído
0 references
15 August 2026
0 references
