Results 181 to 190 of about 58,220 (206)

Silver—Russell syndrome

1996
The exact incidence of this syndrome is not known, but cases have been reported from many parts of the world. All races and ethnic groups seem to be susceptible and both boys and girls seem to be affected equally. (However, there has been an X-linked Silver syndrome described, which has similar characteristics, but which, due to the mode of inheritance,
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Silver-Russell Syndrome following in Vitro Fertilization [PDF]

Pediatric and Developmental Pathology, 2008
[No abstract available]
Douzgou S, Mingarelli R, Tarani L, De Crescenzo A, RICCIO, Andrea   +4 more
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Cleft Hand in Silver–Russell Syndrome

Journal of Hand Surgery, 1988
A case of Silver-Russell Syndrome with a typical cleft hand is presented. The association of cleft hand with this syndrome has never been reported before.
S, Mahmud, K, Namba, K, Sameshima, Y, Nakashima, R, Nishino   +4 more
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The Silver-Russell syndrome.

Acta paediatrica Belgica, 1977
Sir .—Marks and Bergeson ( Am J Dis Child 131:447,1977) have reviewed the literature on the Silver and Russell syndromes and conclude that the reported cases are variants of the same syndrome. Since I have been a vocal advocate of the opposite point of view, 1,2 it seems only fair that I should point out that Cumming et al 3 have effectively spiked my ...
M, Vanderschueren-Lodeweyckx, R, Eeckels, E, Eggermont, G, Fabry   +3 more
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Silver-Russell Syndrome With Unusual Findings

Pediatrics, 1987
In 1953, Silver et al1 described a syndrome of short stature and low birth weight with hemihypertrophy and abnormal sexual development. Independently, in 1954, Russell2 described a condition with similar findings, but his description emphasized disproportionately short arms, maternal difficulty during pregnancy, and craniofacial dysostosis.
K K, Hansen, L A, Latson, B A, Buehler, L A, Latson   +3 more
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Autosomal recessive Silver-Russell syndrome

Clinical Dysmorphology, 1992
Six children (5 male, 1 female) of normal first cousin Arab parents were found to have Silver-Russell syndrome. Manifestations included intrauterine and postnatal growth retardation, lateral asymmetry, relatively large head, small triangular face with prominent ears, clinodactyly of the fifth fingers, disproportionate toes, and normal psychomotor ...
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Diagnostic Proceeding in Silver-Russell Syndrome

Molecular Diagnosis, 2005
Silver-Russell syndrome (SRS) describes a uniform malformation syndrome characterized by pre- and postnatal growth restriction (10% of SRS patients.
Thomas, Eggermann, Esther, Meyer, Michael B, Ranke, Martin, Holder, Stefanie, Spranger, Klaus, Zerres, Hartmut A, Wollmann   +6 more
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Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients

Journal of Medical Genetics, 2009
Background Silver–Russell syndrome (SRS, OMIM 180860) features fetal and postnatal growth restriction and variable dysmorphisms. Genetic and epigenetic aberrations on chromosomes 7 and 11 are commonly found in SRS. However, a large fraction of SRS cases remain with unknown genetic aetiology.
Sara, Bruce, Katariina, Hannula-Jouppi, Mari, Puoskari, Ingegerd, Fransson, Kalle O J, Simola, Marita, Lipsanen-Nyman, Juha, Kere   +6 more
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Silver-Russell Syndrome

Nihon rinsho. Japanese journal of clinical medicine, 2006
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THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION

Wiadomości Lekarskie
Silver-Russell syndrome (SRS) –is an orphan disease characterized by intrauterine and postnatal growth retardation. Children have special phenotypes, difficulties in feeding, the threat of insulin resistance, hypoglycemia, and accelerated sexual ...
N. Gromnatska, M. Iskiv
semanticscholar   +1 more source