Schneiderman Prelims Vol-I. qxd

CONGENITAL
Aplasia cutis congenita – without associated anomalies
Textbook of Neonatal Dermatology, p.129, 2001; extensive scalp
ulcer 
AD 141:554–556, 2005
Aplasia cutis congenita in surviving co-twins 
Ped Derm
18:511–515, 2001
Bart’s syndrome – congenital localized absence of skin with
epidermolysis bullosa 
AD 93:293–304, 1966
Congenital absence of skin 
JAAD 2:203–206, 1980
Epidermal necrosis, intrauterine 
Textbook of Neonatal
Dermatology, p.149, 2001; JAAD 38:712–715, 1998
Noma neonatorum – deep ulcers with bone loss, mutilation of
nose, lips, intraorally, anus, genitalia; Pseudomonas,
malnutrition, immunodeficiency 
Textbook of Neonatal
Dermatology, p.149, 2001
Porokeratosis – congenital linear porokeratosis 
Ped Derm
12:318–322, 1995
Occult spinal dysraphism – aplasia cutis congenita-like lesion
J Pediatr 96:687–689, 1980
DEGENERATIVE DISEASES
Digital mucous cyst
Hereditary sensory neuropathy – plantar ulcers 
Int J Dermatol
23:664–668, 1984
Hypesthesia following encephalitis
Neurotrophic ulcers (mal perforans) (Charcot foot); including
those associated with neuropathies – on metatarsal heads and
heels with underlying sinsus tract to joint or subfascial abscess
Rook p.2775, 1998, Sixth Edition
Peripheral neuropathy – painless acral cutaneous ulcers with
deformity 
Rook p.2775, 1998, Sixth Edition
Reflex sympathetic dystrophy 
JAAD 35:843–845, 1996;
AD 127:1541–1544, 1991
Syringomyelia – painless ulcer 
Ghatan p.26, 2002, Second Edition
Trophic ulcers
Acrodystrophic neuropathy of Bureau and Barriere
Alcoholism
Amantadine-induced peripheral neuropathy
Autonomic trophic disorder of the cerebral hemispheres
Beta thalassemia major and intermedia
Carpal tunnel syndrome
Cauda equina syndrome
Charcot–Marie–Tooth syndrome, type 2A
Chronic obliterating arteriopathies
Compression syndrome
Congenital acro-osteolysis
Congenital dyserythropoietic anemia type II
Cutaneous–mucous trophic disorder
Diabetes mellitus
Distal hyperirrigation syndrome
Familial amyloid polyneuropathy type I
Giaccai syndrome
Gilbert’s syndrome
Hereditary sensory and autonomic neuropathies (HSAN), four
types
Hereditary spastic paraplegia with sensory neuropathy
Klinefelter’s syndrome
Klippel–Trenaunay syndrome
Leprosy
Lipomeningocoele
Multiple sclerosis
Multiple symmetric lipomatosis
Neuroacropathy
Peripheral arterial occlusive disease (Fontaine stage III, IV) 
Peripheral neuropathy
Poliomyelitis
Post-external fixation in quadriplegia
Post-femoropopliteal shunt
Post-keratoplasty
Post-retroperitoneoscopic lumbar sympathectomy
Post-spinal anesthesia
Post-surgery of trigeminal nerve
Post-varicose vein surgery
Reflex sympathetic dystrophy
Rheumatoid arthritis
Spina bifida
Split cord malformation with meningomyelocele (complex
spina bifida) 
Syringomyelia
Tabes dorsalis
Trigeminal trophic syndrome (Wallenberg’s syndrome) 
Ulcerative-mutilating acropathy – inherited (Thavenard’s
syndrome) or acquired (Bureau–Barriere syndrome) 
Venous insufficiency
Werner’s syndrome with torpid trophic ulcera cruris