About KBG Syndrome

Kbg Syndrome, also known as macrodontia, mental retardation, characteristic facies, short stature, and skeletal anomalies, is related to hypertelorism and 16q24. 3 microdeletion syndrome. An important gene associated with Kbg Syndrome is ANKRD11 (Ankyrin Repeat Domain Containing 11), and among its related pathways/superpathways are Chromatin Regulation / Acetylation and 22q11. 2 copy number variation syndrome. Affiliated tissues include bone, heart and kidney, and related phenotypes are scoliosis and short neck

Major Symptoms of KBG Syndrome



* Headache

* Fatigue

* Weakness

* Tremors

* Restlessness

* Muscle weakness

* Nausea

* Diarrhea

* Vomiting

* Abdominal pain

* Vision changes

* Dizziness

* Staggering

* Fainting

* Fatigue

* Restlessness

* Palpitations

* Arthritis

* Enlarged heart

* Shortness of breath

* Swollen legs

* Dizziness

* Nausea

* Fatigue

* Restlessness

* Muscle weakness

* Vision changes

* Abdominal pain

* Fatigue

* Shortness of breath

* Swollen feet

* Dizziness

* Nausea

* Restlessness

Suitable Lifestyle for People with KBG Syndrome

For patients with KBG syndrome, lifestyle adaptability varies depending on individual differences, but generally speaking, patients are recommended to maintain a regular schedule, ensure adequate sleep, perform appropriate exercise, and maintain a good mood. In terms of diet, you should avoid greasy, spicy, and irritating foods, and eat more light and easy-to-digest foods such as vegetables, fruits, and whole grains. In addition, regular examination and treatment should be carried out to ensure that the condition is effectively controlled.

Other Diseases

Cat Eye Syndrome ICF Syndrome H Syndrome Dry Eye Syndrome FG Syndrome NDH Syndrome Down Syndrome 3C Syndrome 3-M Syndrome Hypoventilation Syndrome

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