Renal hypodysplasia and unilateral ovarian agenesis in the Penta-X syndrome
We report the case of a 3‐year‐old penta‐X female with two previously undescribed anomalies: hypoplastic kidney and absent ipsilateral ovary. The gross and histologic structure of the contralateral ovary was normal, suggesting that adults with this syndrome may be fertile.
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Veröffentlicht in: | American journal of medical genetics 1980, Vol.6 (2), p.153-162 |
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container_title | American journal of medical genetics |
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creator | Toussi, Tahmouresse Halal, Fahed Lesage, Robert Delorme, Fernand Bergeron, André Opitz, John M. |
description | We report the case of a 3‐year‐old penta‐X female with two previously undescribed anomalies: hypoplastic kidney and absent ipsilateral ovary. The gross and histologic structure of the contralateral ovary was normal, suggesting that adults with this syndrome may be fertile. |
doi_str_mv | 10.1002/ajmg.1320060209 |
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J. Med. Genet</addtitle><description>We report the case of a 3‐year‐old penta‐X female with two previously undescribed anomalies: hypoplastic kidney and absent ipsilateral ovary. 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subjects | agenesis of ovary congenital hypotonia mental retardation multiple congenital anomalies syndrome pentasomy X renal hypodysplasia shortness of stature |
title | Renal hypodysplasia and unilateral ovarian agenesis in the Penta-X syndrome |
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