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Genetic disorders

Children

Beckwith-Wiedemann Syndrome: Causes, Signs & Diagnosis

Dr. Hareem Sajid -
Beckwith-Wiedemann Syndrome (BWS) is a rare congenital disorder that causes abnormal growth in infants and children. It involves...
Blood

Glanzmann Thrombasthenia: Causes, Symptoms & Diagnosis

Dr. Hareem Sajid -
Glanzmann thrombasthenia (GT) is a bleeding disorder caused by impaired platelet function. It’s characterized by lifelong episodes of...
Congenital Disorders

Cohen Syndrome: Rare Genetic Disorder Explained

Dr. Moeez Nadeem -
Cohen syndrome, also known as Norio syndrome in Finnish populations, is a rare autosomal recessive genetic disorder that...
Genetic disorders

Castleman Disease: Uncovering the Mysterious Illness

Shama Mukhtar -
Castleman disease (CD) refers to a rare, nonclonal lymphoproliferative disorder characterized by abnormal overgrowth of lymph node tissue....

Crigler Najjar Syndrome: Understanding a Rare Condition

Children Dr. Ayesha Maqsood Dr. Ayesha Maqsood -
Crigler Najjar syndrome is an inherited disorder in which genetic abnormality causes a poor function of enzymes involved in bilirubin processing, and it leads...
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