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The Journal of Clinical Endocrinology & Metabolism, 1948
A SYNDROME of decreased stature, sexual infantilism, congenital webbing of the neck and cubitus valgus was described by Turner in 1938 (1). All of his seven patients were females and ranged in height from 50 to 56 inches and were between the ages of 15 and 23 years.
R B, GREENBLATT, H E, NIEBURGS
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A SYNDROME of decreased stature, sexual infantilism, congenital webbing of the neck and cubitus valgus was described by Turner in 1938 (1). All of his seven patients were females and ranged in height from 50 to 56 inches and were between the ages of 15 and 23 years.
R B, GREENBLATT, H E, NIEBURGS
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Australasian Radiology, 1986
SUMMARYA foetus in utero was found to have a small cystic hygroma on the back of its neck at 17/18 weeks. Chromosome analysis revealed a female karyotype 45, X diagnostic of Turner's Syndrome.
P W, Verco, J, Barbary, C, Enthoven
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SUMMARYA foetus in utero was found to have a small cystic hygroma on the back of its neck at 17/18 weeks. Chromosome analysis revealed a female karyotype 45, X diagnostic of Turner's Syndrome.
P W, Verco, J, Barbary, C, Enthoven
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Klinefelter Syndrome and Turner Syndrome
Pediatrics In Review, 20211. Carole Samango-Sprouse, EdD*,†,‡ 2. Sophia Q. Song, BA‡ 3. Angela E. Lin, MD§ 4. Cynthia M. Powell, MD¶ 5. Andrea L. Gropman, MD*,** 1. *George Washington University, Washington, DC 2. †Florida International University, Miami, FL 3. ‡Department of Research, The Focus Foundation, Davidsonville, MD 4.
Carole, Samango-Sprouse +4 more
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?ere?evskij-Turner's syndrome or Turner's syndrome
Human Genetics, 1977Attention is drawn to the original description by Seresevskij in 1925 of what later in American and Western European literature asually has been called Turner's syndrome, based on the description by Turner in 1938.
N C, Lonberg, J, Nielsen
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Clinical Genetics, 1992
Verschraegen‐Spae M‐R, Depypere H, Speleman F, Dhondt M, De Paepe A. Familial Turner syndrome. Clin Genet 1992:41: 218–220.A 28‐year‐old Turner female with secondary amenorrhea is described, who showed 45,X/46,X,del(Xp) mosaicism in her blood lymphocytes and a 46,X,del(Xp) karyotype only in her ovaries.
M R, Verschraegen-Spae +4 more
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Verschraegen‐Spae M‐R, Depypere H, Speleman F, Dhondt M, De Paepe A. Familial Turner syndrome. Clin Genet 1992:41: 218–220.A 28‐year‐old Turner female with secondary amenorrhea is described, who showed 45,X/46,X,del(Xp) mosaicism in her blood lymphocytes and a 46,X,del(Xp) karyotype only in her ovaries.
M R, Verschraegen-Spae +4 more
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The Indian Journal of Pediatrics, 1968
A case of Turner’s syndrome is reported whose chief features were stunted growth, short neck, cubitus valgus, sexual infantilism, bilaterally longitudinal depressions in front of the chest wall and shortening of the fourth toes, including the metatarsals and phalanges. The sex chromatin was negative i.e. genetic male.
K D, Mohanta +3 more
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A case of Turner’s syndrome is reported whose chief features were stunted growth, short neck, cubitus valgus, sexual infantilism, bilaterally longitudinal depressions in front of the chest wall and shortening of the fourth toes, including the metatarsals and phalanges. The sex chromatin was negative i.e. genetic male.
K D, Mohanta +3 more
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Annals of Internal Medicine, 1978
Seven women in three generations of a family have been affected by Turner syndrome. Turner phenotype in this family is the result of deletion of the entire short arm of one X chromosome. The short arm deletion is transmitted by carriers of a balanced X-1 translocation.
D A, Leichtman +5 more
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Seven women in three generations of a family have been affected by Turner syndrome. Turner phenotype in this family is the result of deletion of the entire short arm of one X chromosome. The short arm deletion is transmitted by carriers of a balanced X-1 translocation.
D A, Leichtman +5 more
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Endocrinology and Metabolism Clinics of North America, 1991
Turner syndrome occurs in 1 of every 2000 to 5000 live female births and is now recognized to encompass a broad range of chromosomal karyotypes and clinical phenotypes. Many of these individuals appear completely normal save for their short stature. This article reviews the major clinical and physiologic abnormalities that can occur and places special ...
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Turner syndrome occurs in 1 of every 2000 to 5000 live female births and is now recognized to encompass a broad range of chromosomal karyotypes and clinical phenotypes. Many of these individuals appear completely normal save for their short stature. This article reviews the major clinical and physiologic abnormalities that can occur and places special ...
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Journal of Clinical Epidemiology, 1998
Turner syndrome afflicts approximately 50 per 100,000 females and is characterized by retarded growth, gonadal dysgenesis, and infertility. Much attention has been focused on growth and growth promoting therapies, while less is known about the natural course of the syndrome, especially in adulthood.
Gravholt, C H +3 more
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Turner syndrome afflicts approximately 50 per 100,000 females and is characterized by retarded growth, gonadal dysgenesis, and infertility. Much attention has been focused on growth and growth promoting therapies, while less is known about the natural course of the syndrome, especially in adulthood.
Gravholt, C H +3 more
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Graefe's Archive for Clinical and Experimental Ophthalmology, 2002
Turner's syndrome is a chromosomal abnormality where phenotypic females have either a missing X chromosome or a structural aberration of the X chromosome. Several ocular diseases have been associated with Turner's syndrome in the past, including one case only of proven iridocyclitis.In this study we report the clinical findings of three females with ...
M. ACCORINTI +3 more
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Turner's syndrome is a chromosomal abnormality where phenotypic females have either a missing X chromosome or a structural aberration of the X chromosome. Several ocular diseases have been associated with Turner's syndrome in the past, including one case only of proven iridocyclitis.In this study we report the clinical findings of three females with ...
M. ACCORINTI +3 more
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