Craniometaphyseal dysplasia (CMD) is a rare congenital bone dysplasia with abnormal bony overgrowth leading to characteristic facial features and cranial nerve compression. We present a 10-year-old child with bony swelling at the nasal root since birth along with decreased hearing in both ears. She had normal developmental milestones and intelligence. On examination, she had bossing of forehead with very broad nasal root, short septum, hypertelorism and epicanthic folds. CT scan with 3D reconstruction revealed grossly thickened calvarium and hyperostosis and sclerosis of the cranial base. As the major concern of the parents was cosmetic, craniofacial reconstruction was performed with good cosmetic outcom
Cleidocranial dysplasia (CCD) is a bone disorder with cranial malformations, dental abnormaliti...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...
Craniometaphyseal dysplasia (CMD) is a rare congenital bone dysplasia with abnormal bony overgrowth...
We report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented with a h...
AbstractWe report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented ...
Craniometaphyseal dysplasia (CMD) is a rare genetically transmitted bone dysplasia characterized by ...
Craniometaphyseal dysplasia (CMD) is a rare genetic skeletal disorder, whose biological understandin...
Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth ...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
Craniometaphyseal dysplasia (CMD) is a very rare bone disorder of unknown etiology. It is characteri...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease, which is caused by muta...
Cleidocranial dysplasia is a rare autosomal dominant condition with generalized dysplasia of bone, c...
none3AIM: Cleidocranial dysplasia (CCD) is a rare disorder that is inherited as an autosomal genetic...
Introduction: Cleido-cranial dysplasia (CCD) is a rare congenital disorder with an autosomal dominan...
Cleidocranial dysplasia (CCD) is a bone disorder with cranial malformations, dental abnormaliti...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...
Craniometaphyseal dysplasia (CMD) is a rare congenital bone dysplasia with abnormal bony overgrowth...
We report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented with a h...
AbstractWe report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented ...
Craniometaphyseal dysplasia (CMD) is a rare genetically transmitted bone dysplasia characterized by ...
Craniometaphyseal dysplasia (CMD) is a rare genetic skeletal disorder, whose biological understandin...
Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth ...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
Craniometaphyseal dysplasia (CMD) is a very rare bone disorder of unknown etiology. It is characteri...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease, which is caused by muta...
Cleidocranial dysplasia is a rare autosomal dominant condition with generalized dysplasia of bone, c...
none3AIM: Cleidocranial dysplasia (CCD) is a rare disorder that is inherited as an autosomal genetic...
Introduction: Cleido-cranial dysplasia (CCD) is a rare congenital disorder with an autosomal dominan...
Cleidocranial dysplasia (CCD) is a bone disorder with cranial malformations, dental abnormaliti...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...