Schneiderman Prelims Vol-I. qxd

SYNDROMES
Acrogeria 
Rook p.2513, 1998, Sixth Edition
Ataxia telangiectasia 
Rook p.2749, 1998, Sixth Edition
Carcinoid syndrome – sclerodermoid changes 
Rook p.2717,
1998, Sixth Edition; sclerosis of the legs BJD 129:222–223,
1993; scleroderma-like lesions Arch Int Med 131:550–553, 1973
Cataracts, alopecia, and sclerodactyly – ectodermal dysplasia
syndrome on the island of Rodrigues 
Am J Med Genet
32:500–532, 1989
Cervical rib syndrome – indurated edema 
Rook p.2512–2513,
1998, Sixth Edition
Cockayne’s syndrome
Congenital ichthyosiform dermatosis with linear keratotic
flexural papules and sclerosing palmoplantar keratoderma
AD 125:103–106, 1989
Congenital fascial dystrophy (stiff skin syndrome) (Parana hard
skin syndrome) – autosomal recessive; hirsutism, limited joint
mobility, localized areas of stony hard skin of buttocks and legs
Ped Derm 20:339–341, 2003; Ped Derm 19:67–72, 2002;
JAAD 43:797–802, 2000; JAAD 21:943–50, 1989; Ped Derm
3:48–53, 1985; Ped Derm 2:87–97, 1984
Congenital generalized fibromatosis 
Ghatan p.33, 2002,
Second Edition
Dento-oculo-cutaneous syndrome – pigmented and indurated
interphalangeal joints, thick and wide philtrum, ectropion, dental
abnormalities, dystrophic fingernails 
Int J Dermatol 12:285–289,
1973
Dermochondrocorneal dystrophy – Francois’ syndrome – hands
AD 124:424–428, 1988
Diffuse lipomatosis – autosomal dominant 
Proc Greenwood
Genet Center 3:56–64, 1984
Familial histiocytic dermoarthritis of Zayd
Familial scleroderma-like fingers (familial sclerodactyly)
JAAD 33:302–304, 1995
Fibroblastic rheumatism – sudden onset, symmetrical
polyarthritis, sclerodactyly with retraction of palmar
aponeurosis, Raynaud’s phenomenon, pulmonary fibrosis; skin
lesions resolve spontaneously 
AD 131:710–712, 1995
Flynn–Aird syndrome – progressive sensorineural deafness,
neurologic signs and symptoms, sclerodermoid changes