Abstract
Acromicria is a rare medical condition manifested by the abnormal underdevelopment of small size of the extremities particularly the habds and feet. Etiology of acromicria include congenital acromicria, aquired acromicria, endocrine disorders and nutritional deficiencies. Clinical presentations are small hands and feet, delayed growth. Limited mobility and bone abnormalities. Diagnosis is based on imaging studies, genetic testing, hormone tests and radio logical assessment. Treatment is linked to the genetic causes, hormonal causes, medical monitoring and orthopedic interventions.
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