Schneiderman Prelims Vol-I. qxd

PSYCHOCUTANEOUS DISEASE
Anorexia nervosa – diffuse non-scarring alopecia 
Rook p.2795,
1998, Sixth Edition
Delusions of parasitosis
Factitial alopecia 
Ped Derm 21:205–211, 2004; Rook
p.2800–2802, 1998, Sixth Edition
Trichoteiromania – obsessive rubbing of hair 
Dtsch Dermatol
Ges 1:22–28, 2003; Eur J Dermatol 11:369–371, 2001
Trichotemnomania – obsessive cutting of hair 
JAAD
52:157–159, 2005; Hautarzt 22:335–337, 1971; Hautarzt
19:551–553, 1968
Trichotillomania 
JAAD 46:807–821, 2002; Curr
Prob Derm VIII:97–136, 1996; J Clin Psychol Psychiatry
32:401–409, 1991; follicular hyperkeratosis BJD
145:1034–1035, 2001
SYNDROMES
ACD mental retardation syndrome 
Am J Med Genet
13:383–387, 1982
Acrocephalopolysyndactyly
Adams–Oliver syndrome
Alopecia–anosmia–deafness–hypogonadism syndrome 
Am J
Med Genet 26:925–927, 1987
Alopecia, epilepsy, oligophrenia syndrome of Moynahan 
Proc R
Soc Med 55:411–412, 1962
Alopecia, contractures, mental retardation, dwarfism syndrome
Alopecia, keratosis pilaris, cataracts, and psoriasis 
JAAD
21:351–357, 1989
Alopecia–mental retardation syndrome
J Med Genet 20:64–65,
1983
Alopecia, psychomotor epilepsy, pyorrhea, mental retardation
Clin Genet 11:13–17, 1977
Alopecia and structural abnormalities of the nose and hands
Alopecia–onychodysplasia–hypohidrosis–deafness
syndrome – small teeth, thick dystrophic toenails,
hypohidrosis, hyperkeratosis of palms and soles, elbows and
knees, sensorineural deafness 
Hum Hered 27:127–337, 1977
Chondroectodermal dysplasia (Ellis van Creveld syndrome)
Ped 26:301–309, 1960
Coffin–Siris syndrome
Am J Dis Child 119:433–439, 1970
Hidrotic ectodermal dysplasia (Clouston’s syndrome) 
J Can
Med Ass 21:18–31, 1929
Langer–Gideon syndrome 
Orthop Rev 21:31–35, 1992
Larsen’s syndrome 
J Ped 37:574–581, 1950
Neu–Laxova syndrome – resembles harlequin fetus;
resembles restrictive dermopathy
Oral facial digital syndrome 
Arch Dis Child 44:729–731, 1969
Tricho–onychodental dysplasia 
Oral Surg 46:376–385, 1978
Trichorhinophalangeal syndrome 
JAAD 31:331–336, 1994
Anhidrotic ectodermal dysplasia (Christ–Siemens–Touraine
syndrome) 
J Dermatol 26:44–47, 1999; X-linked recessive –
premature aged appearance with soft, dry, finely wrinkled
skin, especially around eyes; absent or reduced sweating,
sparse fine scalp hair, eyebrows, eyelashes, and total or partial
anodontia with conical pointed teeth
Ped Derm 19:226, 2002;
J Med Genet 28:181–185, 1991; autosomal recessive
Ped Derm 7:242, 1990; carrier state of X-linked anhidrotic
ectodermal dysplasia
Ankyloblepharon, ectodermal dysplasia, and cleft lip and
palate syndrome (AEC syndrome) (Hay–Wells syndrome) –
hair sparse, coarse, wiry or absent, dystrophic nails,
dystrophic widely spaced pointed teeth are shed early,
chronic scalp erosions in early childhood 
Ped Derm
19:226, 2002; Ped Derm 14:149–150, 1997; BJD
94:287–289, 1976
Anonychia with bizarre flexural pigmentation – autosomal
dominant, absent nails, dry peeling palmoplantar skin, coarse
and sparse frontal hair; mottled hyper- and hypopigmentation of
the axillae, groin, and natal cleft 
BJD 92:469–474, 1975
ANOTHER syndrome – alopecia, nail dystrophy, ophthalmic
complications, thyroid dysfunction, hypohidrosis, ephelides and
enteropathy, respiratory tract infections 
Clin Genet 35:237–242,
1989; J Pediatr 108:109–111, 1986
Atrichia congenita with papular lesions – autosomal
recessive; infantile hair loss, follicular papules; follicular
cysts and milia-like lesions 
AD 139:1591–1596, 2003; JAAD
47:519–523, 2002; Ped Derm 19:155–158, 2002; Eur J
Dermatol 11:375–377, 2001; Dermatology 185:284–288,
1992; Dermatologica 108:114–121, 1954; atrichia with keratin
cysts – face, neck, scalp then trunk and extremities 
Ann DV
121:802–804, 1994
Baraitser syndrome (premature aging with short stature and
pigmented nevi) – lack of facial subcutaneous fat, fine hair,
hypospadias, dental abnormalities, hepatomegaly 
J Med Genet
25:53–56, 1988; J Med Genet 20:64–75, 1983