Scientists have discovered the first case of cystic fibrosis in a newborn
The Indian team of researchers says they have discovered a case of CF in a baby born to a woman who had cystic Fibrosis, but the study was done in India.
It says the child was born with cystic CF.
The baby’s mother had cystitis, a disease in which a person’s skin is infected with cysts.
The team has now identified the virus that caused the cyst infection in the newborn, according to the report published in The Lancet Infectious Diseases.
The case is described as “a promising case for cystic cystic disease in neonates.”
The infant’s condition is still unknown, the report says.
It notes that there are some similarities to a child with CF who has had a genetic mutation in the CF gene, and a few other conditions.
But the team is also focusing on what the infant is doing at this time, and how it might respond to the infection.
Researchers are also looking at what other conditions could be causing the baby’s illness.
It’s not known yet how the child’s infection will develop, but it is possible the baby could be born with the virus.
The researchers said in their report that the child had no known previous medical history of CF.
They say the infant’s mother was a normal, healthy, and active mother.
They are also studying other possible causes for the infection, including the baby being in close contact with another child with cystosis, or the mother’s previous CF symptoms.
This type of cyst is rare in people, but when it does occur, the symptoms include pain and fever, fatigue, and abdominal pain.
In addition to the CF virus, the infant also had a gene mutation that caused an abnormal growth in the baby cells.
The mutation is believed to cause the baby to have a mutation in cystic filaments in the membranes of their mitochondria, the power plants that power cells.
Mitochondria are the main power plants in cells and make up 90 percent of a cell’s mass.
They have many functions in cells, including producing energy, maintaining proper cell growth, and transporting nutrients.
The report adds that this gene mutation is likely to be more common in people with CF, as the mutation occurs only in people who are genetically predisposed to the disease.
They add that if the mutation is caused by CF, it could be passed to a baby and cause the disease as well.
The study also notes that the baby did not have a history of previous cystic-fibrosis cases in her family, and no genetic tests were taken to determine whether her baby had CF.
In a press release, the researchers say the case is “a positive case and represents a promising first step in the ongoing investigation of the causes of cytic CF.”
They also note that other researchers have reported the first cases of CF, but they did not identify the cause.
The Indian study comes on the heels of a study published in the journal PLOS One, which also reported the discovery of the first CF in newborns.
The authors said the new case is the first to be found in a child.
The research team was led by scientists at India’s Institute of Tropical Diseases and Epidemiology, and the baby was born on March 12, 2019.
The parents were members of a small community of people with cytic fibrosis, who live in a village in the eastern state of Tamil Nadu, the study said.
In the study, the team of scientists identified the mutation as the CF variant, which was not found in any previous studies of children with CF.
Researchers also looked into a gene known to be associated with CF and found it to be a mutation that occurs in CF patients in people of Asian ancestry.
The genetic mutation appears to be common in CF, and there have been reports of mutations occurring in people in both groups.
The new case could also have been related to the mutation, researchers said.
“We are in a very early stage of our investigation, but we suspect that this child may have a familial variant of the CF disease, but this variant was not identified until now,” said Dr. Amit Chaudhary, a researcher in the study.
“It could have been caused by the CF-associated mutation, but until this mutation is identified we will not be able to predict the extent of the risk.”
The researchers have since sent a sample of the child to the Indian Institute of Cytology and Venereology for DNA testing.
The results of the DNA test should be available by the end of the month.