Diprosopus

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Diprosopus[edit | edit source]

Diprosopus, also known as craniofacial duplication, is a rare congenital disorder characterized by the duplication of facial features. Diprosopus, also known as craniofacial duplication, is a rare congenital disorder characterized by the duplication of facial features. It is a form of conjoined twinning where the embryo does not fully separate during development, resulting in the formation of two faces on a single head. This condition is extremely rare, with only a few documented cases in medical literature.

Causes[edit | edit source]

The exact cause of diprosopus is not well understood. It is believed to occur due to abnormalities during the early stages of embryonic development. Some researchers suggest that genetic factors and environmental influences may play a role in the development of this condition. However, more research is needed to determine the precise causes.

Symptoms[edit | edit source]

The most prominent symptom of diprosopus is the presence of two faces on a single head. The duplicated facial features can vary in their degree of development and symmetry. In some cases, both faces may have fully formed features, including eyes, noses, mouths, and ears. In other cases, one face may be more developed than the other, resulting in asymmetry. Other associated symptoms may include cleft lip and palate, abnormal skull shape, and neurological abnormalities.

Diagnosis[edit | edit source]

Diagnosing diprosopus can be challenging, especially during prenatal stages. It is often detected during routine ultrasound examinations, where the presence of duplicated facial features can be observed. After birth, a physical examination and medical imaging techniques such as CT scans or MRI may be used to confirm the diagnosis.

Treatment[edit | edit source]

There is no specific treatment for diprosopus. The management of this condition involves a multidisciplinary approach, including surgical interventions, feeding support, and addressing associated medical issues. Surgical procedures may be performed to correct any craniofacial abnormalities or to improve the functionality of the duplicated facial features. However, the prognosis for individuals with diprosopus is generally poor, and the condition is often incompatible with long-term survival.

Notable Cases[edit | edit source]

Lali Singh, a girl with diprosopus, gained international attention in 2008. Diprosopus is an extremely rare condition, and there have been only a few documented cases in medical literature. One notable case is that of Lali Singh, a girl from India who gained international attention in 2008. Lali had two faces, each with its own set of eyes, nose, and mouth. Despite her condition, Lali was able to live a relatively normal life with the support of her family and medical professionals.

References[edit | edit source]


See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD