Mullerian duct anomalies - limb anomalies (Q94182): Difference between revisions

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Síndrome de Anomalias do ducto de Müller-anomalias dos membros é caracterizada pela associação de ducto de Muller (do septo vaginal à duplicação completa do útero e vagina nas mulheres e micropênis nos homens) e anomalias dos membros distais (de polidactilia pós-axial a hipoplasia grave dos membros superiores com mão dividida )
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Müllerian duct anomalies - limb anomalies syndrome is characterised by the association of Mullerian duct (from vaginal septum to complete duplication of uterus and vagina in females, and micropenis in males) and distal limb anomalies (from postaxial polydactyly to severe upper limb hypoplasia with split hand).

Revision as of 09:18, 16 August 2026

Müllerian duct anomalies - limb anomalies syndrome is characterised by the association of Mullerian duct (from vaginal septum to complete duplication of uterus and vagina in females, and micropenis in males) and distal limb anomalies (from postaxial polydactyly to severe upper limb hypoplasia with split hand).
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ID_1418232947
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    Mullerian duct anomalies - limb anomalies
    Müllerian duct anomalies - limb anomalies syndrome is characterised by the association of Mullerian duct (from vaginal septum to complete duplication of uterus and vagina in females, and micropenis in males) and distal limb anomalies (from postaxial polydactyly to severe upper limb hypoplasia with split hand).

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