Apert syndrome is a genetic condition that is present from birth. It involves the fusion of certain bones in the skull, which can cause problems with brain development and health. 1. There is no established or proven cure for Apert syndrome; however, there are treatments available to manage the symptoms. 2. In some cases, surgery can be used to correct the bones and facial deformities associated with the con  Read More

Cure or Medication for campomelic dysplasia Campomelic dysplasia has no known treatment; alternatively, it is treated or prevented. The structural problems may potentially be corrected by surgical techniques. The following are the treatments for Campomelic dysplasia. 1. PEEP: Positive end-expiratory pressure (PEEP), a mechanical breathing aid, may help affected people with respiratory issues.  Read More

Pierre Robin sequence is characterized by an unusually small lower jaw (micrognathia) and downward displacement of the tongue (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate); both the soft and hard palate can be affected.  Read More

Nager Acrofacial Dysostosis Syndrome is a rare genetically inherited disorder where the newborn shows signs of craniofacial malformations. It's mostly associated with irregularities of the thumb and forearms. In particular circumstances, underdevelopment of bones in the face and hands is visible, while poor development of the cheek and jaw area is seen. Weak movement in the elbow is Cures/medications for Nager Acro  Read More

Pierre Robin sequence is characterized by an unusually small lower jaw (micrognathia) and downward displacement of the tongue (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate); both the soft and hard palate can be affected.  Read More

Pierre Robin sequence is characterized by an unusually small lower jaw (micrognathia) and downward displacement of the tongue (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate); both the soft and hard palate can be affected.  Read More

Pierre Robin sequence is characterized by an unusually small lower jaw (micrognathia) and downward displacement of the tongue (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate); both the soft and hard palate can be affected.  Read More

Pierre Robin sequence is characterized by an unusually small lower jaw (micrognathia) and downward displacement of the tongue (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate); both the soft and hard palate can be affected.  Read More