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(1968)
Vergleichende klinische und morphologische Untersuchungen zwischen einem Neugeboren mit
Address: Prof. Dr. N . Freire-Maia Dept. of Genetics Federal University of Paranh P.O. Box A A 80.000 Curitiba
M. Bajor (1974)
Red cell acid phosphatase polymorphism in Hungary.Human heredity, 24 3
C. Witkop (1971)
Heterogeneity in gingival fibromatosis.Birth defects original article series, 7 7
A. Salisbury (1974)
The National Foundation ‐ March of DimesClinical Genetics, 5
J. Herrmann, E. Gilbert, J. Opitz (1977)
Dysplasia, Malformations and Cancer, Especially with Respect to the Wiedemann-Beckwith Syndrome
(1973)
Hypertrichosis lanuginosa. Birth Defects
R. Suskind, N. Esterly (1971)
Congenital hypertrichosis universalis.Birth defects original article series, 7 8
G. Winter, M. Simpkiss (1974)
Hypertrichosis with hereditary gingival hyperplasiaArchives of Disease in Childhood, 49
Beighton (1970)
Congenital hypertrichosis lanuginosaArch. Dermatol., 101
Hypertrichosis lanuginosa (without gingival hyperplasia) is described in a mother and son; the latter also had photophobia, infantile genitalia, growth retardation, hypotension, low IQ and dental abnormalities (hyperdontia, permanence of deciduous and delayed eruption of permanent teeth). Both have normal dermatoglyphics. Some clinical findings are discussed. The presence of this syndrome in a mother and son supports an autosomal mode of inheritance (with variable expressivity). Hypertrichosis lanuginosa is a pure monomultidysplasia and may be classified with the tricho-odontic sub-group of the ectodermal dysplasias.
Clinical Genetics – Wiley
Published: Nov 1, 1976
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