Patient Information:

• Name: Kreem I.A. Khalafalla
• Diagnosis: Hereditary Ataxia
• Date of Birth (D.O.B): June 29, 1989
• Gender: Male
• Country: Sudan

Treatment: Neural Growth Factor Therapy for Hereditary Ataxia, Cerebral Metabolism Improvement Treatment, Neurotrophic Treatment, Traditional Chinese Medicine (TCM), and Rehabilitation Therapy

Medical History:
Kreem was admitted to Puhua International Hospital on May 31st, 2011, presenting with unsteady walking that had progressed over seven years. He was diagnosed with hereditary ataxia.

Medical Condition before Neural Growth Factor Treatment for Hereditary Ataxia:
At admission:

• Gait: Difficult to walk even with assistance; often lost balance and fell
• Fatigue: Easily fatigued
• Limb coordination: Poor, especially in the legs; clumsy alternating movements

Treatment Course:
Kreem underwent Neural Growth Factor Therapy targeting cerebral metabolism improvement and neurotrophic effects. This was combined with Traditional Chinese Medicine (TCM) and comprehensive rehabilitation therapy.

Post-Treatment Updates:
Following Neural Growth Factor Treatment for Hereditary Ataxia:

• Gait: Improved steadiness while standing and walking; better balance control
• Endurance: Able to walk longer distances with reduced fatigue
• Historical trip: During his hospitalization, Kreem visited the Great Wall of China and Tiananmen Square, climbing the wall and enjoying a long walk without significant fatigue
• Physical examination: Upon discharge, Kreem's fingers showed increased flexibility compared to his condition upon admission

Patient & Family Feedback:
Kreem and his parents were highly satisfied with the results of his Neural Growth Factor Therapy. They expressed optimism regarding further improvements in Kreem's condition after discharge from Puhua Hospital.