Article
Variable expressivity of the phenotype in two families with brachydactyly type E, craniofacial dysmorphism, short stature and delayed bone age caused by novel heterozygous mutations in the PTHLH gene.
Journal of human genetics - 1 May 2016
Jamsheer Aleksander, Sowińska-Seidler Anna, Olech Ewelina M, Socha Magdalena, Kozłowski Kazimierz, Pyrkosz Antoni, Trzeciak Tomasz, Materna-Kiryluk Anna, Latos-Bieleńska Anna
Abstract excerpt
Brachydactyly refers to shortening of digits due to hypoplasia or aplasia of bones forming the hands and/or feet. Isolated brachydactyly type E (BDE), which is characterized by shortened metacarpals and/or metatarsals, results in a small proportion of patients from HOXD13 or PTHLH mutations, although in the majority of cases molecular lesion remains unknown. BDE, like other brachydactylies, shows clinical...
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