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KBG syndrome

KBG syndrome is a rare condition characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay. To date, KBG syndrome has been reported in 45 patients. Clinical features observed in more than half of patie...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Brancati, Francesco, Sarkozy, Anna, Dallapiccola, Bruno
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2006
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1764006/
https://ncbi.nlm.nih.gov/pubmed/17163996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-1-50
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