Baby Born with Waxy, Shiny, Plastic-like Skin Gets New Lease of Life

A baby born prematurely with a rare and potentially life threatening skin disease has been given a new lease of life by doctors at Panipat, Haryana.
The baby boy was born at 36 weeks to a couple from Zirakpur in Punjab. He suffered with a congenital skin condition
The baby boy was born at 36 weeks to a couple from Zirakpur in Punjab. He suffered with a congenital skin conditionRepresentational image. Pixabay

A baby born prematurely with a rare and potentially life threatening skin disease has been given a new lease of life by doctors at Panipat, Haryana.

The baby boy was born at 36 weeks to a couple from Zirakpur in Punjab. He suffered with a congenital skin condition, characterised by tight, waxy, shiny skin resembling plastic -- known as Collodion Syndrome.

This autosomal recessive genetic disorder is a dermatological emergency, with an estimated incidence of 1 in 50,000 to 100,000 births, said Cloudnine Newborn Centre in Panipat.

The baby had red skin covered by a thick membrane known as the Collodion Membrane on the chest, upper and lower extremities, with eyelid and lip eversion, and deformed ears.

Daily monitoring of weight, serum electrolytes, and input/output was performed, and IV fluids were administered to maintain hydration and prevent electrolyte imbalances.

"The Collodion baby syndrome is a rare and potentially life-threatening dermatological condition. Very few infants with this disorder survive the first week of life and have almost a 50 per cent chance of mortality," Dr Shalin Parikh, Consultant Neonatologist & Pediatrician at Cloudnine Group of Hospitals, Panipat, told IANS.

The baby required oxygen support and was nursed in an incubator with 70 per cent humidity. A dermatology consult was obtained, and skin emollients were initiated.

Genetic testing of parents showed the absence of consanguinity or family history.
Genetic testing of parents showed the absence of consanguinity or family history. Pixabay

The baby's infection screen was positive, and a 2-week course of high-grade IV antibiotics was given.

Daily monitoring of weight, serum electrolytes, and input/output was performed, and IV fluids were administered to maintain hydration and prevent electrolyte imbalances.

Over time, the eyelid and lip eversion improved with the shedding of the Collodion skin membrane, the doctors said.

Genetic testing of parents showed the absence of consanguinity or family history. The doctors counselled the parents regarding the autosomal recessive inheritance pattern of most cases of congenital ichthyosis.

"This case was challenging as the infant had acquired an infection during his admission outside, and there was respiratory distress. It required multi-disciplinary management from skin and ENT specialists. With timely interventions and parents' trust in our team, we were able to save the baby's life," Parikh said.

"The infant was discharged after 10 days of NICU stay at a weight of 2.2 kg. On follow-up, the infant had an excellent skin texture and skin texture gain," the doctor added.  (PB/NewsGram)

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The baby boy was born at 36 weeks to a couple from Zirakpur in Punjab. He suffered with a congenital skin condition
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