Esophageal Progeria, Little Boy Treated Finally Expert Team Physician Location: West Sulawesi Your Diet Guide

Esophageal Progeria, Little Boy Treated Finally Expert Team Physician Location: West Sulawesi

Posted by Taylah Degotardi 26 Jun, 2011

Remember the kid in the 10-year-old dwarf Polewali Mandar, western Sulawesi, which has a weight no more than 7 pounds?. Remaining body weight is now 5 pounds, although his age is growing. Ega Savitri siriodadi boy from the village, subdistrict wonomulyo / Polewali is sentenced to suffer the disease progeria or genes that cause growth abnormalities have penuaaan EGA premature prematurely, are now being handled team of expert doctors. Ega was diagnosed with Hutchinson-gliford syndrome or progeria disease of childhood. A number of citizens and social institutions that empathy was mengelurkan unable to help on this family. Ega Savitri , the boy is sentenced to suffer stunted growth abnormalities of genes or disease-gliford Hutchinson syndrome or progeria disease of childhood, is now getting special attention pediatrician Polewali Mandar hospital. progeria disease suffered by EGA also called Hutchinson-gliford syndrome. The disease is characterized by growth failure in the first year. At the age of the original EGA year growth looks healthy. The photos at Ega-old this year looks like a healthy fit kids his age, but later his mother was surprised that instead of growing larger EGA, seriing accretion age. Despite his age continues to grow, but even more weight menuurun EGA. Three months ago, EGA recorded weight 7 pounds, when it checked at the nearest health center. Finally after a team of expert doctors weighed / three days ago, now lives EGA weight 5 kilograms. Compare the physical growth Ega with her sister, Nila Savitri standing beside him. Tilapia are now sitting on the bench grade 2 SD. Weight and height appear larger. Head of Polewali Mandar health department, Dr. Ayub AliAli who went to the house in the village of Ega Siriodadi, sub wonomulyo, Polewali, Thursday today, confirming if Ega Savitri suffers from progeria or gangguanpertumbuhan physical disease that causes premature penuaaan EGA experienced before time. “Ega suffer from abnormalities of genes or progeria, the disease causes premature aging Ega experience prematurely. The team doctor was trying to help Ega order to recover at least can walk “the doctor said Ayub ali Team pediatrician is currently working to assist the growth of the EGA to be run as normal as children age. Murniati, the biological mother who faithfully takes care of Ega since birth, hopes there is change in physical growth of his future after team doctors handled, at least Ega could walk meet kebutuhanya such as eating and drinking alone. “I hope EGA could walk like other children,” said Murniati, EGA biological mother wished her son could be healed. As a year-old child, everywhere Ega must be picked up parents or family. Let alone walk normally like his age / eat and drink just to make ends meet / they need help from others. Since this poor kid crowded reported a variety of media, a number of social institutions that empathize incessantly visited the house Ega. In addition to the family was unable to give assistance is also mmeberi encouragement to both parents to care for her son steadfastly. Andi Masri, public figures proclaiming Polewali empathize with families Ega. Andi Masri took the family to visit formed friendships and Ega in the house. “As human beings we are certainly worthy of empathy to participate alleviate or encouragement to fellow members in order to stay motivated to live,” said Andi Masri. As expectations of both parents Ega, number of citizens who see and empathize with the family life EGA also pray that someday could grow normally and could walk like other children.

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