Branchio-Oculo-Facial Syndrome BOFS: is a rare genetic disorder where defects are apparent on the head and the neck because they characterize malformations of the eyes and ears.
Ectrodactyly: includes missing central fingers and toes from the said organs. It often affects the middle fingers, but more digits than one could be missing.
Progeria HGPS: Hutchinson-Gilford syndrome, Progeria is one of the rarest genetic disorders that causes children to age rapidly, usually starting.
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Acrocallosal Syndrome ACLS: a distinctive number of those affected by Acrocallosal Syndrome, making this one of the rarest defects present at birth.
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Smith-Lemli-Opitz Syndrome: is a disordered development of many different parts of the body, usually having characteristics of autism. Infants.
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Adams-Oliver Syndrome AOS: is a rare disease characterized by missing skin on the scalp, limb abnormalities, heart defects, and webbed fingers and toes.
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Conjoined Twins Siamese Twins: The rarest type of twins is a condition called Conjoined twins, where twins’ bodies are physically fused together even before birth.
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Tibial Hemimelia: is a condition that, in rare cases, occurs at birth, characterized by a missing tibia or a shorter than normal shinbone in the child’s legs.
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Phocomelia: Phocomelia occurs in infants born with undeveloped or completely absent arms or legs. This defect causes a flipper-like appearance of the limbs.