Hydrometrocolpos, postaxial polydactyly, congenital heart disease, and anomalies of the gastrointestinal and genitourinary tracts: a rare autosomal recessive syndrome

Nine cases with the hydrometrocolpospolydactyly syndrome (4 males, 5 females) from four unrelated families are presented. Leading symptoms of this rare disorder were hydrocolpos and postaxial polydactyly. Three affected girls had urinary hydrocolpos without vaginal septum or imperforate hymen, one h...

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Veröffentlicht in:European journal of pediatrics 1981-07, Vol.136 (3), p.297-305
Hauptverfasser: Goecke, T, Dopfer, R, Huenges, R, Conzelmann, W, Feller, A, Majewski, F
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Sprache:eng
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