Gonadal dysgenesis; Bonnevie-Ullrich-Turner syndrome with elevated urinary gonadotropins in a nine-year-old child.
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Body Fluids↗
Biomedical subjects
H K SILVER
Publications and source records attributed to H K SILVER.
Sterilization and preservation of formulas for infants.
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Humans↗
Involvement of the central nervous system in infectious mononucleosis in childhood.
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Central Nervous System↗
Roentgenographic examination of infants in an incubator; a new device insuring environmental constancy.
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Humans↗
Symmetric form of Bonnevie-Ullrich syndrome (syndrome of webbing of the neck, lymphangiectatic edema, shortness of stature, cubitus valgus and deformities of the toes).
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Body Height↗
Congenital toxoplasmosis; report of case with cataract, atypical vasopressin-sensitive diabetes insipidus, and marked eosinophilia.
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Cataract↗
Reticuloendotheliosis and myeloproliferative disorders: presentation of a case intermediate between these disorders and a discussion of their interrelationships.
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Bone Marrow↗
A technique for roentgenographic examination of newborn, premature, or ill infants without removal from an incubator.
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Child↗
Ovarian agenesis (congenital aplastic ovaries) in children.
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Female↗
Ovarian agenesis (congenitally aplastic ovaries) in a 3-year-old female.
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Congenital Abnormalities↗
Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins.
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Body Height↗
Extreme eosinophilia, increased blood heterophile-agglutination titer, and hyperglobulinemia.
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Agglutination↗
The lipoproteins of serum in infancy and childhood. I. Lipoproteins in normal children.
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Child↗
The lipoproteins of serum in infancy and childhood. II. Lipoprotein levels in juvenile diabetes mellitus.
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Diabetes Mellitus, Type 1↗
Fanconi syndrome; multiple congenital anomalies with hypoplastic anemia.
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Abnormalities, Multiple↗
Mediterranean anemia.
There are two forms of Mediterranean anemia, one mild, the other severe. The major variety is characterized by pronounced anemia and systemic changes. In the minor form, usually there is no anemia or other clinical abnormality. The milder disease is relatively common in Italians, but both forms may occur in persons of non-Mediterranean ancestry, as well as in those who come from areas adjoining the Mediterranean Sea. Diagnosis of the disease is made on the basis of history, clinical observation, roentgen studies of the bones, and exceptionally painstaking laboratory tests. Periodic transfusions of whole blood are necessary for persons with the more severe form of the disease.
Anemia↗
Syndrome of ovarian agenesis (congenitally aplastic ovaries): short stature, multiple congenital abnormalities and high urinary gonadotropins in a two year, eight month old female.
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Dwarfism↗
Mediterranean anemia in children of non-Mediterranean ancestry.
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Anemia↗