Total: 2 |
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PMID (PMCID) | ||
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24092917 |
FEMALE | Child |
A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype. | ||
Zweier C, Kraus C, Brueton L, Cole T, Degenhardt F, Engels H, Gillessen-Kaesbach G, Graul-Neumann L, Horn D, Hoyer J, Just W, Rauch A, Reis A, Wollnik B, Zeschnigk M, Ludecke HJ, Wieczorek D. J Med Genet. 2013;50(12):838-47. |
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Borjeson-Forssman-Lehmann syndrome (BFLS) is an X-linked recessive intellectual disability (ID) disorder caused by mutations in the PHF6 gene and characterised by variable cognitive impairment, a distinct facial gestalt, obesity, and hypogonadism. | ||
19187102 |
MALE | Adult |
Behavioural phenotype in Borjeson-Forssman-Lehmann syndrome. | ||
de Winter CF, van Dijk F, Stolker JJ, Hennekam RC. J Intellect Disabil Res. 2009;53(4):319-28. |
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Borjeson-Forssman-Lehmann syndrome (BFLs) is an X-linked inherited disorder characterised by unusual facial features, abnormal fat distribution and intellectual disability. |