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Article

Dunnigan-Kobberling syndrome: an autosomal dominant form of partial lipodystrophy.

QJM : monthly journal of the Association of Physicians - 1 Jan 1997

Jackson S N, Howlett T A, McNally P G, O'Rahilly S, Trembath R C

Abstract excerpt

Dunnigan-Kobberling syndrome is a form of partial lipodystrophy characterized by sparing of the face. Despite descriptions of six families since 1974, details of total body adipose tissue distribution and studies of carbohydrate and fat metabolism are lacking. The mode of inheritance also remains unclear, with most authors favouring an X-linked dominant transmission lethal in the hemizygous male. We examined 23...

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Identifiers

PMID: 9093586
DOI: 10.1093/qjmed/90.1.27

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Dunnigan-Kobberling syndrome: an autosomal dominant form of partial lipodystrophy.PMID 9093586Read ↗

Type 1 familial partial lipodystrophy: understanding the Köbberling syndrome.Semantic proximity Read ↗

Dunnigan-type familial partial lipodystrophy associated with the heterozygous R482W mutation in LMNA gene - case study of three women from one family.Semantic proximity Read ↗

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Gender differences in the prevalence of metabolic complications in familial partial lipodystrophy (Dunnigan variety).Semantic proximity Read ↗

Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22.Semantic proximity Read ↗

Lipodystrophic Laminopathies: From Dunnigan Disease to Progeroid Syndromes.Semantic proximity Read ↗

Nuclear envelope-related lipodystrophies.Semantic proximity Read ↗

A-type lamin-linked lipodystrophies.Semantic proximity Read ↗

Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C.Semantic proximity Read ↗

Endoplasmic reticulum stress activation in adipose tissue induces metabolic syndrome in individuals with familial partial lipodystrophy of the Dunnigan typeSemantic proximity Read ↗

Phenotypic gender differences in subjects with familial partial lipodystrophy (Dunnigan variety) due to a nuclear lamin A/C R482W mutation.Semantic proximity Read ↗

The molecular basis of genetic lipodystrophies.Semantic proximity Read ↗

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