A voyage for a cure

September 24, 2017 12:02 am | Updated 12:02 am IST

Shalini Yadav, 16, known as the "snake girl" poses in Marbella on September 15, 2017. 
Shalini, who suffers recessive lamellar ichthyosis and sheds her skin every six weeks due to a rare condition, is to get life-improving treatment in southern Spain. / AFP PHOTO / JORGE GUERRERO

Shalini Yadav, 16, known as the "snake girl" poses in Marbella on September 15, 2017. Shalini, who suffers recessive lamellar ichthyosis and sheds her skin every six weeks due to a rare condition, is to get life-improving treatment in southern Spain. / AFP PHOTO / JORGE GUERRERO

Spain to her rescue: Shalini Yadav, a teenager from Chhatarpur district in Madhya Pradesh, and afflicted with a rare disorder, lamellar ichthyosis (fish-like scales), from birth, is to undergo treatment for free at a hospital in the Spanish city of Málaga. A report on her plight appeared across world media and and a few Indian journalists and fund-raisers played a crucial role in facilitating her treatment. The girl is now at Hospital Universitario Virgen de la Victoria. Lamellar ichthyosis is a condition that mainly aects the skin. Infants with this condition are typically born with a tight, clear sheath covering their skin called a collodion membrane. Such people have large, dark, plate-like scales. Affected infants could develop infections, an excessive loss of fluids (dehydration), and respiratory problems. These individuals may also have hair loss, abnormally formed fingernails and toenails, a decreased ability to sweat, an increased sensitivity to heat, and a thickening of the skin on the palms of the hands and soles of the feet. * AFP

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