We report on four additional unrelated cases of Bohring-Opitz syndrome with the highly characteristic phenotype of facial anomalies including bulging forehead over the metopic Suture, frontal nevus flammeus, exophthalmos, hypertelorism, upslanting palpebral fissures, and cleft lip and/or palate, as well as flexion deformities of the upper limbs, multiple other anomalies, and severe failure to thrive. We also update the clinical outcome of the patients reported in the original article by Bohring et al. [Am J Med Genet 85:438-446] and critically review the subsequently published cases considered to have Bohring-Opitz syndrome. (c) 2006 Wiley-Liss, Inc
Opitz G BBB syndrome is a rare condition characterized by the 3 major anomalies of hypertelorism, cl...
Background Bohring-Opitz syndrome (BOS) is a rare genetic disorder characterised by a recognisable c...
SUMMARY: Opitz syndrome is a rare autosomal recessive disorder of cholesterol metabolism associ-ated...
We report on four additional unrelated cases of Bohring-Opitz syndrome with the highly characteristi...
In 1999, Bohring et al. reported a new syndrome clinically distinguishable from cases with C syndrom...
Bohring-Opitz syndrome (BOS) is a rare genetic disorder, characterized by feeding difficulties, deve...
Bohring-Opitz syndrome (BOS) is a rare condition characterized by facial anomalies, multiple malform...
The diagnostic challenge of Bohring-Opitz Syndrome, a rare genetic disorder has haunted clinicians f...
Bohring–Opitz syndrome (BOS) was first described by Bohring et al. [1999]. The authors reported four...
Opitz G BBB syndrome is a rare condition characterized by the 3 major anomalies of hypertelorism, cl...
Background Bohring-Opitz syndrome (BOS) is a rare genetic disorder characterised by a recognisable c...
SUMMARY: Opitz syndrome is a rare autosomal recessive disorder of cholesterol metabolism associ-ated...
We report on four additional unrelated cases of Bohring-Opitz syndrome with the highly characteristi...
In 1999, Bohring et al. reported a new syndrome clinically distinguishable from cases with C syndrom...
Bohring-Opitz syndrome (BOS) is a rare genetic disorder, characterized by feeding difficulties, deve...
Bohring-Opitz syndrome (BOS) is a rare condition characterized by facial anomalies, multiple malform...
The diagnostic challenge of Bohring-Opitz Syndrome, a rare genetic disorder has haunted clinicians f...
Bohring–Opitz syndrome (BOS) was first described by Bohring et al. [1999]. The authors reported four...
Opitz G BBB syndrome is a rare condition characterized by the 3 major anomalies of hypertelorism, cl...
Background Bohring-Opitz syndrome (BOS) is a rare genetic disorder characterised by a recognisable c...
SUMMARY: Opitz syndrome is a rare autosomal recessive disorder of cholesterol metabolism associ-ated...