Medical

otopalatodigital syndrome

o·to·pal·a·to·dig·i·tal syn·drome

[MIM*311300]
conductive hearing impairment, cleft palate, broad nasal root, and frontal bossing, wide spacing of toes, broad thumbs and great toes, and often other signs of generalized bone dysplasia; X-linked recessive inheritance.
Farlex Partner Medical Dictionary © Farlex 2012

o·to·pal·a·to·dig·i·tal syn·drome

(ōtō-pală-tō-diji-tăl sindrōm) [MIM*311300]
Conductive hearing impairment, cleft palate, broad nasal root, frontal bossing, wide spacing of toes, broad thumbs and great toes, and often other signs of generalized bone dysplasia.
Medical Dictionary for the Dental Professions © Farlex 2012
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References in periodicals archive
Instead of raising money for new soccer gear or team trips that year, Wormdahl created what has since become an annual fundraiser for Dering's son, Jake, who was born with otopalatodigital syndrome type II, also known as OPD.
The inspiration behind the gift is 2-year-old Jake Kennedy Dering, who was born with a medical condition known as Otopalatodigital Syndrome Type II (OPD).
His condition is called Otopalatodigital Syndrome type II, also known as OPD; it's a rare genetic disorder, with only 30-some known cases worldwide, with only a few of those surviving past infancy.
[2] reported that MNS is characterized by the most severe phenotypes in the spectrum of otopalatodigital syndromes and by the exclusive location of causal missense mutations in the exon 22 hotspot.
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