Börjeson-Forssman-Lehmann syndrome (Q87498): Difference between revisions

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Revision as of 13:08, 15 August 2026

Borjeson-Forssman-Lehmann syndrome is characterised by the association of intellectual deficit with endocrine anomalies, epilepsy, hypogonadism and facial dysmorphism.
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ID_2101263588
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    Börjeson-Forssman-Lehmann syndrome
    Borjeson-Forssman-Lehmann syndrome is characterised by the association of intellectual deficit with endocrine anomalies, epilepsy, hypogonadism and facial dysmorphism.

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      CID11:ID_2101263588
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