Schneiderman Prelims Vol-I. qxd

Partial congenital lipodystrophy – adipose tissue depots variably
affected by lipoatrophy or lipohypertrophy, hepatosplenomegaly,
cardiomyopathy, features of acromegaly or hypertriglyceridemia
Ped Derm 19:267–270, 2002
Miescher’s syndrome – generalized lipodystrophy, acanthosis
nigricans, hypertrichosis, insulin-resistant diabetes
Morfan – mental retardation, peculiar facies 
Am J Med Genet
45:525–528, 1993
Olmsted syndrome 
Int J Derm 36:359–360, 1997; Sem Derm
14:145–151, 1995
Prader–Willi syndrome 
JAAD 21:461–469, 1989
Pseudoacromegaly syndrome – type A insulin resistance
syndrome with acral enlargement, muscle hypertrophy, widened
teeth spacing, muscle cramps 
Ped Derm 19:267–270, 2002
Rabson–Mendenhall syndrome – autosomal recessive;
insulin-resistant diabetes mellitus, growth retardation,
fissured tongue, unusual facies (prominent jaw), dental
precocity, hypertrichosis, acanthosis nigricans, onychauxis
(thick fingernails), abdominal protuberance and phallic
enlargement, mentally precocious, early dentition, premature
sexual development, pineal hyperplasia, hyperplasia of the
adrenal cortex 
BJD 147:1096–1011, 2002; Ped Derm
19:267–270, 2002
Rud’s syndrome – ichthyosis, epilepsy, mental retardation,
retinitis pigmentosa
SADDAN syndrome – autosomal dominant; short stature,
severe tibial bowing, severe achondroplasia with profound
developmental delay and acanthosis nigricans 
BJD
147:1096–1011, 2002; Am J Med Genet 85:53–65, 1999
Sjögren–Larsson syndrome – acanthosis nigricans-like lesions
Ped Derm 20:180–182, 2003
Stein–Leventhal syndrome (polycystic ovarian syndrome) 
Thanatophoric dysplasia – autosomal dominant; micromelic
dwarfism; defect in FGFR3 
BJD 147:1096–1011, 2002
Total congenital lipoatrophy – severe insulin resistance with
Type A features, hepatosplenomegaly, cardiomyopathy,
features of acromegaly, hypertriglyceridemia, or genital
hypertrophy 
Ped Derm 19:267–270, 2002