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WARNING: The photo of the baby is graphic and may be upsetting. You can view the photo here . The baby suffers from cyclopia , one of the rarest birth defects that often causes children to die ...
Of the 660,000 congenital syphilis cases reported in 2016, 143,000 resulted in deaths of unborn babies, 61,000 deaths of newborn babies, 41,000 low birth weights or preterm births, and 109,000 young children diagnosed with congenital syphilis. [15] Around 75% were from the WHO's African and Eastern Mediterranean regions. [2]
Individual rates vary greatly dependent upon multiple factors: size of hernia, organs involved, additional birth defects and/or genetic problems, amount of lung growth, age and size at birth, type of treatments, timing of treatments, complications (such as infections) and lack of lung function. [citation needed]
defects of genes on chromosome 3 and 18. Seckel syndrome , or microcephalic primordial dwarfism (also known as bird-headed dwarfism , Harper's syndrome , Virchow–Seckel dwarfism and bird-headed dwarf of Seckel [ 1 ] ) is an extremely rare congenital nanosomic disorder.
But on January 11, when Fisher gave birth, doctor's diagnosed her baby with a rare condition called Treacher Collins syndrome, which is a rare congenital disorder characterized by facial, such as ...
A caul is a piece of membrane that can cover a newborn's head and face. [1] Birth with a caul is rare, occurring in less than 1 in 80,000 births. [2] The caul is harmless and is immediately removed by the attending parent, physician, or midwife upon birth of the child.
Heart defects including ventricular septal defect, atrial septal defect, patent ductus arteriosus and coarctation of the aorta may occur in these children. A smaller population will have growth problems and developmental delay, or intellectual disability. [citation needed] [3] Heart defects and cleft lip [4] may also be featured.
Prune belly syndrome is a rare, genetic birth defect affecting about 1 in 40,000 births. [4] About 97% of those affected are male. Prune belly syndrome is a congenital disorder of the urinary system, characterized by a triad of symptoms.