Orofaciodigital syndrome type 2

Oral-facial-digital (OFD) type 2 is characterized by hand and feet deformities, facial deformities, midline cleft of the upper lip and tongue hamartomas.

Median cleft lip

A type of cleft lip presenting as a midline (median) gap in the upper lip.


Total: 2

                       


(per page)
PMID (PMCID)
12000897
 FEMALE Infant
Oral-facial-digital syndrome type II (Mohr syndrome): clinical and genetic manifestations.
Sakai N, Nakakita N, Yamazaki Y, Ui K, Uchinuma E.
J Craniofac Surg. 2002;13(2):321-6.
Mohr syndrome is an autosomal recessive inherited disease characterized by median cleft lip, poly lobed tongue, absence of medial incisors, and polydactyly of hands and feet.
12000897
 FEMALE Infant
Oral-facial-digital syndrome type II (Mohr syndrome): clinical and genetic manifestations.
Sakai N, Nakakita N, Yamazaki Y, Ui K, Uchinuma E.
J Craniofac Surg. 2002;13(2):321-6.
At this time, we observed a Japanese patient of Mohr syndrome with median cleft lip and tongue, hypertrophied frenula, absence of left medial incisor, and bilateral bifidity of great toe.