Case report. Case 1 (Conradi syndrome, autosomal dominant type).
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Chondrodysplasia Punctata↗
Biomedical subjects
M Feingold
Publications and source records attributed to M Feingold.
Normal values for selected physical parameters: an aid to syndrome delineation.
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Adolescent↗
Autosomal dominant inheritance of Caffey disease.
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Genes, Dominant↗
Median cleft face syndrome (frontonasal dysplasia).
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Child, Preschool↗
Letter: Genetic counseling.
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Abnormalities, Multiple↗
Picture of the month: Klippel-Trenaunay-Weber syndrome (angioosteohypertrophy).
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Angiomatosis↗
Picture of the month. Sirenomelia.
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Ectromelia↗
Infantile cirrhosis with hereditary alpha 1 -antitrypsin deficiency. Clinical improvement in two siblings.
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Alanine Transaminase↗
Ocular aspects of Goldenhar's syndrome.
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Abnormalities, Multiple↗
A case of trisomy 9.
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Abnormalities, Multiple↗
Picture of the month. Polyostotic fibrous dysplasia (McCune-Albright syndrome).
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Endocrine System Diseases↗
Picture of the month. Schwartz-Jampel syndrome (Aberfeld syndrome, chondrodystrophic myotonia).
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Abnormalities, Multiple↗
Etiology and pathogenesis of congenital cleft lip and cleft palate, an NIDR state of the art report.
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Abnormalities, Drug-Induced↗
Incontinentia pigmenti (Bloch-Sulzberger syndrome).
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Abnormalities, Multiple↗
Oculocerebrorenal syndrome. (Lowe syndrome).
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Ammonia↗
What every family should know about their genes and are afraid to ask.
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Child↗