Schneiderman Prelims Vol-I. qxd

HYPERTRICHOSIS, LOCALIZED
275
Schneiderman page 200-300.qxd 5/16/2006 6:49 PM Page 275

---

Oral mucosal hair 
JAAD 15:1301–1302, 1986
Trichomegaly – HIV, SLE, latanoprost 
JAAD 48:161–179, 2003
PSYCHOCUTANEOUS DISORDERS
Anorexia nervosa 
Ghatan p.68, 2002, Second Edition
Habit tic
Trichotillomania with trichophagia – presence of hairs within the
mouth 
JAAD 15:614–621, 1986
SYNDROMES
Blepharocheilodontic syndrome – distichiasis 
Am J Med Genet
65:109–112, 1996
Edward’s syndrome (trisomy 18) – cutis laxa of neck,
hypertrichosis of the forehead and back, hemangiomas
J Med Genet 15:48–60, 1978
Familial hirsutism 
Bolognia p.1054, 2003
Familial virilization 
Bolognia p.1054, 2003
HAIR-AN syndrome – acne, muscular physique, alopecia
(hyperandrogenism), hidradenitis suppurativa, insulin-
resistance, acanthosis nigricans 
AD 133:431–433, 1997
Hereditary gingival fibromatosis – autosomal dominant;
hirsutism 
Oral Surg 78:452–454, 1994
Hermansky–Pudlak syndrome – trichomegaly of eyelashes,
eyebrows, and arms
Hurler syndrome and other mucopolysaccharidoses
Hypertrichosis, coarse face, brachydactyly, obesity, and mental
retardation 
Clin Dysmorphol 5:223–229, 1996
Hypomelanosis of Ito 
Dermatology 195:71–72, 1997
Lymphedema–distichiasis syndrome – double row of eyelashes;
periorbital edema, vertebral abnormalities, spinal arachnoid
cysts, congenital heart disease, thoracic duct abnormalities,
hemangiomas, cleft palate, microphthalmia, strabismus, ptosis,
short stature, webbed neck 
Ped Derm 19:139–141, 2002; Hum
Genet 39:113–6, 1977
Neurofibromatosis type I – precocious puberty – 3% of
patients with NF I have optic chiasm tumors 
J Pediatr
126:364–367, 1995
Neurofibromatosis type II – schwannomas
Oculocerebral cutaneous syndrome
Pachyonychia congenita – bushy eyebrows 
Ped Derm
14:491–493, 1997
Persistent adrenarche syndrome – hirsutism 
Bolognia p.1054,
2003
POEMS syndrome (Takatsuki syndrome, Crowe–Fukase
syndrome) – hirsutism, osteosclerotic bone lesions, peripheral
polyneuropathy, hypothyroidism, and hypogonadism;
sclerodermoid changes (thickening of skin), either generalized
or localized (legs), cutaneous angiomas, blue dermal papules
associated with Castleman’s disease (benign reactive
angioendotheliomatosis), diffuse hyperpigmentation,
maculopapular brown-violaceous lesions, purple nodules
JAAD 44:324–329, 2001; JAAD 40:808–812, 1999;
Cutis 61:329–334, 1998; JAAD 21:1061–1068, 1989;
AD 124:695–698, 1988; JAAD 12:961–964, 1985
Reflex sympathetic dystrophy – increased hair growth
Cutis 68:179–182, 2001; JAAD 35:843–845, 1996; Arch Neurol
44:555–561, 1987
Rubinstein–Taybi syndrome – hypertrichosis of back and
shoulders 
JAAD 46:159, 2002
Schwartz–Jampel syndrome – distichiasis 
Am J Med Genet
65:109–112, 1996
Treacher Collins syndrome – facial hypertrichosis