You are viewing a javascript disabled version of the site. Please enable JavaScript for this site to function properly.
Go to navigationGo to searchGo to contents
Go to chapter navigation
Figure 74.1
(a) Generalized lipoatrophy of the upper and lower limbs. (b) Severe lipoatrophy of the buttocks. (From Martinez et al . 2000 [ ]. Reproduced with p...
Figure 74.5
A pro‐opiomelanocortin (POMC) deficient patient and his unaffected sister showing a lack of red hair. The arrows show a C202T mutation leading to a pr...
Figure 74.9
Lipoedema. (From Langendoen et al . 2009 [ ]. Reproduced with permission of John Wiley & Sons.)
Figure 74.2
Clinical features of Albright hereditary osteodystrophy: (a) obesity; (b) round facies; (c) hypoplastic skin lesion; and (d) detailed view of a skin l...
Figure 74.6
Multiple lipomas in association with Proteus syndrome. (From Smithson and Winter 2004 [ ]. Reproduced with permission of John Wiley & Sons.)
Figure 74.3
X‐ray showing brachydactyly in Albright hereditary osteodystrophy [ ].
Figure 74.7
Hereditary panniculitis caused by homozygous ZZ α 1 ‐antitrypsin deficiency. (From Chowdhury et al . 2002 [ ]. Reproduced with permission of John Wi...
Figure 74.4
Gene structure and post‐translational processing of pro‐opiomelanocortin (POMC). POMC in mammals consists of three exons, of which exons 2 and 3 are t...
Figure 74.8
Alpha‐1‐antitrypsin‐deficiency panniculitis (phenotype PiZZ). (From Yesudian et al . 2004 [ ]. Reproduced with permission of John Wiley & Sons Ltd.)...