Cerebral palsy is a common cause of childhood disability. It has a great impact on parents and caregivers, especially when it reoccurs in the same family. Although familial cerebral palsy is relatively uncommon, cases have been reported among children from consanguineous, non-consanguineous marriages and multiple pregnancies suggesting a possible complex genetic mode of inheritance. Physicians need to be aware of the possibility of familial cerebral palsy for early detection and counseling. We describe a rare case of two male siblings from a non-consanguineous marriage affected by cerebral palsy
Acromesomelic dwarfism is a skeletal dysplasia characterized by disproportion-ate short stature with...
SummaryCerebral palsy—the most common physical disability of childhood—is a clinical diagnosis encom...
Background: Cerebral palsy (CP) is a common disabling condition of movement and posture causing acti...
Objective To investigate risks of recurrence of cerebral palsy in family members with various degree...
Familial idiopathic scoliosis with conjugate gaze palsy is a rare auto-somal recessive disorder char...
Cerebral palsy (CP) is defined as any nonprogressive motor deficits resulting from cerebral abnormal...
Aim: To study the prevalence of congenital anomalies among children with cerebral palsy (CP) born at...
Research Problem: What arc the social aspects of cerebral palsy? Objective: To determine the extent ...
Background: Allgrove or AAA (Triple A) syndrome is a rare autosomal recessive disease characterized ...
Abstract: Escobar syndrome also known as non lethal type of multiple pterygiumsyndrome, is character...
Every month we see to be published dozens of scientific papers about etiology and physiopathology of...
Aim: To determine the proportion of children with cerebral palsy (CP) who had major congenital anoma...
Introduction: Split Hand-Foot malformation (SHFM) is a congenital limb defect that affects the centr...
Background: Intellectual disability (ID) can be inherited in families through consanguineous marriag...
Two siblings were referred for workup for progres-sive neurological deterioration. The elder sibling...
Acromesomelic dwarfism is a skeletal dysplasia characterized by disproportion-ate short stature with...
SummaryCerebral palsy—the most common physical disability of childhood—is a clinical diagnosis encom...
Background: Cerebral palsy (CP) is a common disabling condition of movement and posture causing acti...
Objective To investigate risks of recurrence of cerebral palsy in family members with various degree...
Familial idiopathic scoliosis with conjugate gaze palsy is a rare auto-somal recessive disorder char...
Cerebral palsy (CP) is defined as any nonprogressive motor deficits resulting from cerebral abnormal...
Aim: To study the prevalence of congenital anomalies among children with cerebral palsy (CP) born at...
Research Problem: What arc the social aspects of cerebral palsy? Objective: To determine the extent ...
Background: Allgrove or AAA (Triple A) syndrome is a rare autosomal recessive disease characterized ...
Abstract: Escobar syndrome also known as non lethal type of multiple pterygiumsyndrome, is character...
Every month we see to be published dozens of scientific papers about etiology and physiopathology of...
Aim: To determine the proportion of children with cerebral palsy (CP) who had major congenital anoma...
Introduction: Split Hand-Foot malformation (SHFM) is a congenital limb defect that affects the centr...
Background: Intellectual disability (ID) can be inherited in families through consanguineous marriag...
Two siblings were referred for workup for progres-sive neurological deterioration. The elder sibling...
Acromesomelic dwarfism is a skeletal dysplasia characterized by disproportion-ate short stature with...
SummaryCerebral palsy—the most common physical disability of childhood—is a clinical diagnosis encom...
Background: Cerebral palsy (CP) is a common disabling condition of movement and posture causing acti...