Dunnigan familial partial lipodystrophy
| Familial Partial Lipodystrophy, Dunnigan Type | |
|---|---|
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| Autosomal dominant is the manner of inheritance of this condition |
Dunnigan-type familial partial lipodystrophy, also known as FPLD Type II and abbreviated as (FPLD2), is a rare
nuclear lamins A and C.[1] The condition is named after Scottish doctor Matthew Dunnigan, who pioneered early study into the disorder. [4]
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