Ablepharon syndrome is an extremely rare genetic problem that causes severe craniofacial deformities and numerous other abnormalities of the face, genitalia, and skin. The literature regarding this condition is scarce. We present a case of this syndrome with dental manifestations, not reported before, and discuss its characteristics in order to increase the knowledge of this condition among the dental profession
Barber-Say syndrome (BSS) and ablepharon-macrostomia syndrome (AMS) are infrequently reported congen...
ABSTRACT Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of g...
Amelogenesis imperfecta (AI) represents rare tooth anomalies that affect the quality and/or quantity...
Ablepharon-Macrostomia syndrome (AMS) is a rare collection of findings characterized by absent or hy...
none4siBarber-Say syndrome (BSS) and Ablepharon-Macrostomia syndrome (AMS) are congenital malformati...
To date, Fraser syndrome (FS) and Ablepharon macrostomia syndrome (AMS) have been considered distinc...
To date, Fraser syndrome (FS) and Ablepharon macrostomia syndrome (AMS) have been considered distinc...
Teeth are specialized structural components of the craniofacial skeleton. Developmental defects occu...
We report on a 7-year-old girl with unequivocal features of Barber-Say syndrome (BSS): generalized h...
Abstract Beckwith‐Wiedemann syndrome is a complex multisystem disorder that requires collaboration o...
Morquio syndrome is a rare autosomal recessive inherited disease of lysosomal storage defect associa...
Abstract Clinical Description KBG syndrome is characterized by macrodontia of upper central incisors...
Chondroectodermal dysplasia (Ellis-Van Creveld syndrome) is a rare autosomal recessive congenital ab...
Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of genetic or...
Hereditary diseases affecting the skeleton are heterogeneous in etiology and severity. Though many o...
Barber-Say syndrome (BSS) and ablepharon-macrostomia syndrome (AMS) are infrequently reported congen...
ABSTRACT Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of g...
Amelogenesis imperfecta (AI) represents rare tooth anomalies that affect the quality and/or quantity...
Ablepharon-Macrostomia syndrome (AMS) is a rare collection of findings characterized by absent or hy...
none4siBarber-Say syndrome (BSS) and Ablepharon-Macrostomia syndrome (AMS) are congenital malformati...
To date, Fraser syndrome (FS) and Ablepharon macrostomia syndrome (AMS) have been considered distinc...
To date, Fraser syndrome (FS) and Ablepharon macrostomia syndrome (AMS) have been considered distinc...
Teeth are specialized structural components of the craniofacial skeleton. Developmental defects occu...
We report on a 7-year-old girl with unequivocal features of Barber-Say syndrome (BSS): generalized h...
Abstract Beckwith‐Wiedemann syndrome is a complex multisystem disorder that requires collaboration o...
Morquio syndrome is a rare autosomal recessive inherited disease of lysosomal storage defect associa...
Abstract Clinical Description KBG syndrome is characterized by macrodontia of upper central incisors...
Chondroectodermal dysplasia (Ellis-Van Creveld syndrome) is a rare autosomal recessive congenital ab...
Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of genetic or...
Hereditary diseases affecting the skeleton are heterogeneous in etiology and severity. Though many o...
Barber-Say syndrome (BSS) and ablepharon-macrostomia syndrome (AMS) are infrequently reported congen...
ABSTRACT Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of g...
Amelogenesis imperfecta (AI) represents rare tooth anomalies that affect the quality and/or quantity...