Schneiderman Prelims Vol-I. qxd

TRAUMA
Physical trauma
VASCULAR DISORDERS
Aneurysm – cirsoid aneurysm (arteriovenous fistula) – blue
non-pulsatile nodules of nail fold with macrodactyly 
BJD
115:361–366, 1986
Angiodysplasia, localized 
Ann Med Interne (Paris)
140:237–239, 1989
Blue rubber bleb nevus syndrome 
AD 129:1505–1509, 1993
Hemangioma, congenital, subungual – pseudoclubbing 
JAAD
53:S123–126, 2005
Lymphangiosarcoma
Lymphatic malformation
Lymphedema, congenital (Milroy’s disease) or acquired –
chronic 
Ped Derm 17:270–276, 2000
Vascular hamartoma 
Ped Derm 17:270–276, 2000
Vascular malformation 
Textbook of Neonatal Dermatology, p.326,
2001; Klippel–Trenaunay–Weber Ped Derm 17:270–276, 2000
MARFANOID HABITUS
Alpha-2-deficient collagen disease Klin Wschr 52:906–912, 1974
Beals–Hecht syndrome (congenital contractural arachnodactyly) –
autosomal dominant; crumpled ears, arachnodactyly with
congenital joint contractures, confused with Marfan’s syndrome
but no cardiovascular abnormalities 
Am J Med Genet
25:763–773, 1986; J Bone Joint Surg 53:987–993, 1971
Camurati–Engelmann disease type II – progressive diaphyseal
dysplasia with striation of bones; waddling gait, muscle
weakness, intense leg pain 
J Med Genet 107:5–11, 2002
Cataract, microcornea, dental anomalies 
Ophthalmology
86 (10):1764–1793, 1979
Cerebro-oculo-renal syndrome of Bhaskar 
Ophthalmology
86 (10):1764–1793, 1979
Cohen syndrome – mental retardation, congenital hypotonia,
microcephaly, pleasant affect, micrognathia, open mouth with
prominent incisors
Congenital contractural acachnodactyly – joint contractures
(elbows and knees), crumpled ears
Cotlier–Reinglass syndrome 
Ophthalmology 86 (10):1764–1793,
1979
Cowden’s syndrome
Craniostenosis
Cutis laxa – congenital cutis laxa type V with Marfanoid habitus
Ann DV 117:823–824, 1990
Cytoplasmic body and mitochodrial DNA deletion – marfanoid
habitus and perceptive hearing loss 
J Neurol Sci 99:291–300,
1990
Diverticulosis, hernia, retinal detachment 
Ophthalmology 86
(10):1764–1793, 1979
Ehlers–Danlos syndrome type VIa 
JID 103:47S-52S, 1994
Familial Marfan habitus 
Am J Med Genet 62:417–426, 1996