- BloodyCoins
- 33
(since the majority of people with these illnesses do not live to adulthood, most of the footage available of them is sadly of very young children.)
First, a compilation of deformed children-
Dissection on a baby born with Patau syndrome-
Patau syndrome, or Trisomy 13, is the least common of the autosomal trisomy's, after Down syndrome (Trisomy 21. and Edwards syndrome (Trisomy 18). The extra copy of chromosome 13 in Patau syndrome causes severe neurological and heart defects which make it difficult for infants to survive. The exact incidence of Patau syndrome is not known, although it appears to affect females more than males, most likely because male fetuses do not survive until birth. Patau syndrome, like Down syndrome, is associated with increased age of the mother. It may affect individuals of all ethnic backgrounds.
Another biological typo, could not find any info on this one-
Photos of a case of Bartsocas-Papas syndrome:
Bartsocas-Papas syndrome (BPS) is an autosomal recessive syndrome with severe craniofacial, limb, and genital abnormalities. As of 2011, 24 published cases and families were registered in the Orphanet Report Series.
Compared to other disorders characterized by pterygia, the condition is usually more severe and often lethal: most affected patients die in utero or shortly after birth. We report the first Egyptian family with Bartsocas-Papas syndrome comprising three cases; our proband who was a female infant with severe craniofacial and limb anomalies typical of Bartsocas-Papas syndrome, a similarly affected female fetus which died in utero at the 7th gestational month, and a 16-year-old mentally retarded uncle who presented with some of the typical features of Bartsocas-Papas syndrome, including syndactyly, thumb hypoplasia, and microphthalmia.
Baby with severe cyclopia (eyes are fused in the womb):
Indian baby is born with bulging red eyes and holes in place of his nose-
Agent orange babies-
Spina bifida, a spinal cord birth defect that results in incomplete closing of the spine, is associated with exposure to Agent Orange or other herbicides during qualifying service in Vietnam or Korea. The affected child must have been conceived after the Veteran entered Vietnam or the Korean demilitarized zone during the qualifying service period. Children with spina bifida or covered birth defects who are biological children of Veterans with qualifying service may be eligible for compensation, health care, and vocational training. The US Department of Veterans Affairs has recognized that certain birth defects among Veterans' children are associated with their qualifying service in Vietnam or Korea.
Indian baby with microcephaly-
Microcephaly is a condition where a baby’s head is much smaller than expected. During pregnancy, a baby’s head grows because the baby’s brain grows. Microcephaly can occur because a baby’s brain has not developed properly during pregnancy or has stopped growing after birth, which results in a smaller head size. Microcephaly can be an isolated condition, meaning that it can occur with no other major birth defects, or it can occur in combination with other major birth defects.
Baby with harlequin ichthyosis-
Harlequin-type ichthyosis is a rare genetic disorder that results in thickened skin over nearly the entire body at birth. The skin forms large, diamond-shaped plates separated by deep cracks, which affect the shape of the eyelids, nose, mouth, and ears and limit movement of the arms and legs. The disorder is caused by mutations in the ABCA12 gene, which codes for a protein necessary for transporting lipids out of cells in the outermost layer of skin. Diagnosis is often based on appearance at birth and confirmed by genetic testing.
Bonus: deformed cat
His name is Mr. Norris
First, a compilation of deformed children-
Dissection on a baby born with Patau syndrome-
Another biological typo, could not find any info on this one-
Photos of a case of Bartsocas-Papas syndrome:
Bartsocas-Papas syndrome (BPS) is an autosomal recessive syndrome with severe craniofacial, limb, and genital abnormalities. As of 2011, 24 published cases and families were registered in the Orphanet Report Series.
Compared to other disorders characterized by pterygia, the condition is usually more severe and often lethal: most affected patients die in utero or shortly after birth. We report the first Egyptian family with Bartsocas-Papas syndrome comprising three cases; our proband who was a female infant with severe craniofacial and limb anomalies typical of Bartsocas-Papas syndrome, a similarly affected female fetus which died in utero at the 7th gestational month, and a 16-year-old mentally retarded uncle who presented with some of the typical features of Bartsocas-Papas syndrome, including syndactyly, thumb hypoplasia, and microphthalmia.
Baby with severe cyclopia (eyes are fused in the womb):
Indian baby is born with bulging red eyes and holes in place of his nose-
Agent orange babies-
Spina bifida, a spinal cord birth defect that results in incomplete closing of the spine, is associated with exposure to Agent Orange or other herbicides during qualifying service in Vietnam or Korea. The affected child must have been conceived after the Veteran entered Vietnam or the Korean demilitarized zone during the qualifying service period. Children with spina bifida or covered birth defects who are biological children of Veterans with qualifying service may be eligible for compensation, health care, and vocational training. The US Department of Veterans Affairs has recognized that certain birth defects among Veterans' children are associated with their qualifying service in Vietnam or Korea.
Indian baby with microcephaly-
Microcephaly is a condition where a baby’s head is much smaller than expected. During pregnancy, a baby’s head grows because the baby’s brain grows. Microcephaly can occur because a baby’s brain has not developed properly during pregnancy or has stopped growing after birth, which results in a smaller head size. Microcephaly can be an isolated condition, meaning that it can occur with no other major birth defects, or it can occur in combination with other major birth defects.
Baby with harlequin ichthyosis-
Harlequin-type ichthyosis is a rare genetic disorder that results in thickened skin over nearly the entire body at birth. The skin forms large, diamond-shaped plates separated by deep cracks, which affect the shape of the eyelids, nose, mouth, and ears and limit movement of the arms and legs. The disorder is caused by mutations in the ABCA12 gene, which codes for a protein necessary for transporting lipids out of cells in the outermost layer of skin. Diagnosis is often based on appearance at birth and confirmed by genetic testing.
Bonus: deformed cat
His name is Mr. Norris