Schneiderman Prelims Vol-I. qxd

ALOPECIA
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Schneiderman page 1-100.qxd 5/16/2006 6:49 PM Page 37

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Reflex sympathetic dystrophy 
JAAD 35:843–845, 1996; JAAD
22:513–520, 1990; Arch Neurol 44:555–561, 1987
Reiter’s syndrome
Robert’s syndrome (pseudothalidomide syndrome) –
hypotrichosis, growth retardation, cleft lip, mild facial port
wine stain 
JAAD 37:523–549, 1997
Romberg syndrome (facial hemiatrophy) – frontoparietal
alopecia 
Rook p.2016–2017, 1998, Sixth Edition; Arch Neurol
39:44–46, 1982
Rombo syndrome – papules and cysts of the face and trunk,
basal cell carcinomas, vermiculate atrophoderma, milia, sparse
beard hair and thin eyebrows, trichoepitheliomas, peripheral
vasodilatation with cyanosis 
BJD 144:1215–1218, 2001; JAAD
39:853–857, 1998; JAAD 28:1011–1014, 1993; Acta DV
61:497–503, 1981
Rosselli–Gulinetti syndrome (ectodermal dysplasia) –
autosomal recessive, hypohidrosis, fine, dry, sparse scalp hair,
dystrophic nails and teeth, cleft lip and palate, syndactyly,
defects of external genitalia 
Ped Derm 19:226, 2002; J Plast
Surg 14:190–204, 1961
Rothmund–Thomson syndrome (poikiloderma congenitale) –
autosomal recessive; scalp hair sparse and fine 
Rook p.417,
1998, Sixth Edition; Ped Derm 18:210–212, 2001; Am J Med
Genet 22:102:11–17, 2001; Ped Derm 18:210–212, 2001; Ped
Derm 16:59–61, 1999; Dermatol Clin 13:143–150, 1995; JAAD
27:75–762, 1992; JAAD 17:332–338, 1987; Arch Ophthalmol
(
German) 4:159, 1887
Sakati syndrome – patchy alopecia with atrophic skin above
ears, submental linear scars, acrocephalopolysyndactyly, short
limbs, congenital heart disease, abnormally shaped low-set ears,
ear tag, short neck with low hairline 
J Pediatr 79:104–109, 1971
Salamon’s syndrome – woolly hair, hypotrichosis, dystrophic
nails, ophthalmologic abnormalities, everted lower lip,
outstanding ears 
Arch Klin Exp Dermatol 220:564–575, 1964
Satoyoshi syndrome – alopecia areata (universalis) with
progressive painful intermittent muscle spasms, diarrhea or
unusual malabsorption, endocrinopathy with amenorrhea
(hypothalamic dysfunction), very short stature, flexion
contractures, skeletal abnormalities 
Ped Derm 18:406–410,
2001; AD 135:91–92, 1999
Schopf–Schulz–Passarge syndrome – eyelid cysts (apocrine
hidrocystomas), palmoplantar keratoderma, hypotrichosis,
decreased number of teeth, brittle and furrowed nails 
AD
140:231–236, 2004; BJD 127:33–35, 1992; JAAD 10:922–925,
1984; Birth Defects XII:219–221, 1971
Seckel’s syndrome – autosomal recessive; hair sparse and
prematurely gray, growth retardation, beak-like nose, large eyes,
skeletal defects 
Am J Med Genet 12:7–21, 1982
Short anagen syndrome – hypotrichosis; hair that won’t grow long
JAAD 53:S130–134, 2005; BJD 143:612–617, 2000
Sparse brittle hair and spondyloepimetaphyseal dysplasia
Sternal cleft with hemagiomas of the face and anterior trunk
Swirled alopecia (Blaschko-esque) in:
Aplasia cutis congenita
Conradi’s syndrome 
Hum Genet 70:200–206, 1985
Oral–facial–digital syndrome 
JAAD 31:157–190, 1994
Syringomyelia, syringobulbia 
Dermatol Wochenschr
143:543–545, 1961
Taurodontism, oligodontia, sparse hair 
Birth Defects 11:39–50, 1975
Tay syndrome – brittle and sparse hair, progeric appearance,
low birthweight
Ped Derm 19:226, 2002
Thumb deformity and alopecia
Treacher Collins syndrome (mandibulofacial dysostosis) –