Add to ORKGMeckel-Gruber syndrome is a rare autosomal recessive lethal malformation characterised by typical manifestations of occipital encephalocele, bilateral polycystic kidneys and post axial polydactyly. But clinically unsuspected or atypical features may be discovered at autopsy or pathological study. One such rare case, diagnosed by ultrasound scan at 21weeks of gestation was terminated and presented here for discussion, with its phenotypic manifestations detailed by autopsy and histo-pathological examination
by Meckel in 1822, later by Gruber and more recently by Opitz and Howe.1 It is a lethal autosomal re...
We wish to present our case of the rare Meckel-Gruber syndrome, diagnosed prenatally at 18 weeks&rsq...
Meckel–Gruber syndrome (MKS) is a rare autosomal recessive condition with an estimated incidence of ...
Meckel Gruber Syndrome is a rare and lethal autosomal recessive congenital anomaly syndrome, charact...
Meckel-Gruber syndrome is an autosomal recessive disorder, usually lethal, most commonly characteris...
This Paper has been presented for Promotion at the University of KhartoumMeckel-Gruber syndrome is a...
Meckel-Gruber Syndrome (MGS) is a rare autosomal recessive disorder that is characterized by typical...
Meckel Gruber syndrome (MGS) is a rare lethal autosomal recessive disorder. It is characterized by ...
Meckel-Gruber syndrome (MGS) is a rare and lethal autosomal recessive disorder characterized by occi...
Meckel Gruber syndrome is an autosomal recessive disorder, characterized by a combination of renal c...
We report of a case of Meckel Gruber Syndrome (MGS) in a woman, who suffered previously from a pregn...
Meckel gruber syndrome or dysencephalia splanchnocystica, is a rare autosomal recessive disorder cau...
Background: Meckel-Gruber Syndrome (MGS) is a rare autosomal recessive congenital syndrome with tria...
OBJECTIVE: To analyze prenatal sonographic anomalies detected in fetuses with Meckel Gruber syndrome...
Meckel-Gruber syndrome is a monogenic congenital disorder characterized by occipital encephalocele, ...
by Meckel in 1822, later by Gruber and more recently by Opitz and Howe.1 It is a lethal autosomal re...
We wish to present our case of the rare Meckel-Gruber syndrome, diagnosed prenatally at 18 weeks&rsq...
Meckel–Gruber syndrome (MKS) is a rare autosomal recessive condition with an estimated incidence of ...
Meckel Gruber Syndrome is a rare and lethal autosomal recessive congenital anomaly syndrome, charact...
Meckel-Gruber syndrome is an autosomal recessive disorder, usually lethal, most commonly characteris...
This Paper has been presented for Promotion at the University of KhartoumMeckel-Gruber syndrome is a...
Meckel-Gruber Syndrome (MGS) is a rare autosomal recessive disorder that is characterized by typical...
Meckel Gruber syndrome (MGS) is a rare lethal autosomal recessive disorder. It is characterized by ...
Meckel-Gruber syndrome (MGS) is a rare and lethal autosomal recessive disorder characterized by occi...
Meckel Gruber syndrome is an autosomal recessive disorder, characterized by a combination of renal c...
We report of a case of Meckel Gruber Syndrome (MGS) in a woman, who suffered previously from a pregn...
Meckel gruber syndrome or dysencephalia splanchnocystica, is a rare autosomal recessive disorder cau...
Background: Meckel-Gruber Syndrome (MGS) is a rare autosomal recessive congenital syndrome with tria...
OBJECTIVE: To analyze prenatal sonographic anomalies detected in fetuses with Meckel Gruber syndrome...
Meckel-Gruber syndrome is a monogenic congenital disorder characterized by occipital encephalocele, ...
by Meckel in 1822, later by Gruber and more recently by Opitz and Howe.1 It is a lethal autosomal re...
We wish to present our case of the rare Meckel-Gruber syndrome, diagnosed prenatally at 18 weeks&rsq...
Meckel–Gruber syndrome (MKS) is a rare autosomal recessive condition with an estimated incidence of ...