Acrogerie gottron E34.8
Synonym(s)
Acrogerie Gottron family; Family Acrogerie Gottron; Gottron syndrome I; OMIM 201200
History
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Gottron, 1941
Definition
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Probably autosomal recessive or autosomal dominant inherited atrophy of skin and subcutaneous fat tissue.
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Manifestation
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From birth or in the first weeks of life, gynaecotropia with a ratio of 3:1.
Localization
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Face and acra.
Clinic
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Atrophic facial skin, often facial erythema, regional fat loss, frequent scarlatiniform exanthema, micrognathia, acromicity, possibly infantile skeleton of the distal extremities. Combination with systemic scleroderma possible.
Differential diagnosis
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Therapy
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Not known.
Literature
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- Blaszczyk M et al (2000) Acrogeria of the Gottron type in a mother and son. Eur J Dermatol 10: 36-40
- Butenandt O, Christophers E (1970) The Acrogerie (Gottron). German med Vshr 95: 175-178
- Gottron H (1941) Family Acrogeria. Arch Derm 181: 571-583
Recommended articles
Incoming links (6)
Acrogerie gottron, family; Ageing syndromes; Bird face; Gottron syndrome i; Lower leg pigmentation, hereditary atrophy associated with atrophy; Photosensitivity syndromes;Outgoing links (5)
Aplasia cutis congenita (overview); Ehlers-danlos syndrome; Exanthema, scarlatiniformes; Infantile progeria; Scleroderma systemic;Disclaimer
Please ask your physician for a reliable diagnosis. This website is only meant as a reference.
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Prof. Dr. med. Peter Altmeyer