Hairy cutaneous malformation of the palms and soles
JAAD 48:161–179, 2003
Hajdu–Cheney syndrome (osteolysis) – broad eyebrows
(synophrys)
J Periodontol 55:224–229, 1984
Hemihypertrophy with hypertrichosis
JAAD 48:161–179, 2003
Hemimaxillofacial dysplasia (segmental odontomaxillary
dysplasia) (HATS – hemimaxillary enlargement, asymmetry
of face, skin findings) – facial asymmetry, hypertrichosis of
the face, unilateral maxillary enlargement, partial anodontia,
delayed eruption of teeth, gingival
thickening of affected
segment, Becker’s nevus, hairy nevus (hypertrichosis),
lip hypopigmentation, depression of cheek, erythema,
hypoplastic teeth
Ped Derm 21:448–451, 2004; JAAD
48:161–179, 2003; Oral Surg Oral Med Oral Pathol
64:445–448, 1987
Hermansky–Pudlak syndrome – hypertrichosis of the eyebrows,
and trichomegaly of the arms and legs
AD 135:774–780, 1999
Heterotopic brain tissue
Textbook
of Neonatal Dermatology,
p.498,500, 2001
Heterotopic meningeal tissue
Textbook of Neonatal
Dermatology, p.498, 2001
Hirsutism
Hunter’s
syndrome
JAAD 48:161–179, 2003
Hurler’s syndrome
JAAD 48:161–179, 2003
Hypertrichosis cubiti (hairy elbow)
JAAD 48:161–179, 2003;
AD 137:877–884, 2001; Clin Exp Dermatol 24:497–498, 1999
Hypertrichosis, pigmentary retinopathy, and facial anomalies –
lipoatrophy of buttocks
Am J Med Genet 62:386–390, 1996
Hypertrichosis pinnae in babies of diabetic mothers
JAAD 48:161–179, 2003; Indian Pediatr 24:87–89, 1987;
Pediatr 68:745–6, 1981
Hypomelanosis of Ito – focal hypertrichosis
JAAD 48:161–179,
2003; Dermatology 193:63–64, 1996; of genital area or back
Ped Derm 19:536–540, 2002
Kabuki makeup syndrome – long eyelashes
J Pediatr
105:849–850, 1984
Lumbar hypertrichosis
Mal de Meleda – autosomal dominant, autosomal recessive
transgrediens with acral erythema
in glove-like distribution;
hairy palms and soles
Dermatology 203:7–13, 2001;
AD 136:1247–1252, 2000; J Dermatol 27:664–668, 2000;
Dermatologica 171:30–37, 1985
Mandibulofacial dysostosis – distichiasis
Mannosidosis – autosomal recessive; gingival hypertrophy,
macroglossia, coarse features, prognathism, thick eyebrows, low
anterior hairline, deafness, lens opacities, hepatosplenomegaly,
recurrent
respiratory tract infections, muscular hypotonia, mental
retardation
Ped Derm 18:534–536, 2001
Melanocytic nevus, congenital
JAAD 48:161–179, 2003; Rook
p.1733–1735,2892, 1998, Sixth Edition; JAAD 36:409–416, 1997
MELAS syndrome – mitochondrial encephalomyopathy with
lactic acidosis – hypertrichosis of the legs
JAAD 48:161–179,
2003; JAAD 41:469–473, 1999
Meningioma – nodule with overlying alopecia or hypertrichosis
JAAD 46:934–941, 2002; Eur J Pediatr Surg 10:387–389, 2000
Meningocoele, cranial
Textbook of Neonatal Dermatology,
p.498, 2001
Meningothelial hamartoma – hair collar sign and vascular stain
Ped Derm 22:200–205, 2005
Mitochondrial disorders – hypertrichosis of the back or diffusely
on
the back, forearms, and forehead; erythematous
photodistributed eruptions followed by mottled or reticulated
hyperpigmentation; alopecia with or without hair shaft
abnormalities including trichothiodystrophy, trichoschisis, tiger
tail pattern, pili torti, longitudinal grooving, and trichorhexis
nodosa
Pediatrics 103:428–433, 1999
Mucopolysaccharidoses types I, II, III, IV, VI – thick eyebrows
with synophrys
JAAD 37:295–297, 1997; Sanfilippo
syndrome
(mucopolysaccharidosis III)
JAAD 48:161–179, 2003;
Dur J Pediatr 130:251–258, 1979
Neurofibromatosis – plexiform neurofibroma
Curr Prob
Dermatol 13:249–300, 2002
Neurofibroma
JAAD 48:161–179, 2003
Nevoid hypertrichosis
JAAD 48:161–179, 2003; JAAD
39:114–115, 1998; Am J Med Genet 79:195–196, 1998;
Clin Exp Dermatol 16:74, 1991
Nevus lipomatosis superficialis
BJD 87:557–564, 1972
Noonan’s syndrome – downy hypertrichosis on cheeks and
shoulders
AD 114:929–930, 1978
Occult spinal dysraphism – faun tail nevus; dermoid cyst or
sinus, myelomeninocele, diastematomyelia, vertebral
abnormalities, subdural or extradural lipoma, meningioma
JAAD 48:161–179, 2003; Textbook of Neonatal Dermatology,
p.498, 2001; Ped Clin North Am 47:813–823, 2000
Oliver–McFarlane syndrome – trichomegaly with mental
retardation, dwarfism, and pigmentary degeneration of the
retina
JAAD 37:295–297, 1997; Can J Ophthalmol 28:191–193,
1993
Opitz trigonocephaly syndrome – hypertrichosis of forehead;
widow’s peak
Am J Dis Child 129:1348, 1975
Oral hair
Oral Surg 49:530–531, 1980
Penchaszadeh syndrome (nasopalpebral lipoma-coloboma
syndrome)
Am J Med Genet 11:397–410, 1982
Periorbital neurofibroma
Ophthalmology 103:942–948, 1996
Peripheral sensory and motor neuropathy
JAAD 25:767–770,
1991
Phenylketonuria – long eyelashes
Rook p.2812, 1998, Sixth
Edition
Plexiform neurofibroma
Textbook of Neonatal Dermatology,
p.498, 2001
Polycystic ovarian disease
Porphyria – porphyria cutanea tarda –
decreased hepatic
uroporphyrinogen decarboxylase in sporadic and toxic forms,
and decreased enzyme in all tissues in the hereditary form;
accumulation of water soluble 8-, 7-, 6-, 5-, and 4-
carboxylporphyrins; hypertrichosis of cheeks, forehead, and
periorbital regions in about 2/3 of patients with PCT
JAAD
48:161–179, 2003; Rook p.2590,2892, 1998, Sixth Edition;
hepatoerythropoietic porphyria
AD 138:957–960, 2002; AD
116:307–313, 1980; variegate porphyria JAAD 48:161–179,
2003; Rook p.2892, 1998, Sixth Edition hereditary
coproporphyria
BJD 96:549–554, 1977; Q J Med 46:229–241,
1977; BJD 84:301–310, 1971; congenital erythropoietic
porphyria – lanugo hair on extremities, terminal hair on face
Semin Liver Dis 2:154–63, 1982
Primary cutaneous meningioma –
including rudimentary
meningocoele with tuft of hair over vertebral column
J Neurosurg 60:1097–1098, 1984; AD 130:775–777, 1994;
JAAD 30:363–366, 1994
Primary cervical hypertrichosis (anterior cervical and/or midline
posterior cervical) (nevoid hypertrichosis)
AD 137:877–884,
2001
Pigmented hairy epidermal nevus syndrome
Sem Derm
14:111–121, 1995
Primary multifocal hypertrichosis
Eur J Dermatol 11:35–37, 2001
Proteus syndrome
AD 140:947–953, 2004
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