Börjeson-Forssman-Lehmann syndrome (Q87498): Difference between revisions
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A síndrome de Borjeson-Forssman-Lehmann é caracterizada pela associação de déficit intelectual com anomalias endócrinas, epilepsia, hipogonadismo e dismorfismo facial. | |||
| description / en | description / en | ||
Borjeson-Forssman-Lehmann syndrome is characterised by the association of intellectual deficit with endocrine anomalies, epilepsy, hypogonadism and facial dysmorphism. | |||
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2101263588 |
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| English | Börjeson-Forssman-Lehmann syndrome |
Borjeson-Forssman-Lehmann syndrome is characterised by the association of intellectual deficit with endocrine anomalies, epilepsy, hypogonadism and facial dysmorphism. |
