Wednesday, November 24, 2010

Kembar Siam Dan Ketahui Jenis-Jenisnya


Kembar siam atau kembar bercantum adalah keadaan anak kembar yang tubuh keduanya bersatu. Hal ini terjadi apabila zigot dari bayi kembar seiras gagal terpisah secara sempurna. Kemunculan kes kembar siam diperkirakan adalah satu dalam 200,000 kelahiran. Yang mampu bertahan hidup berkisar antara 5% dan 25%, dan kebanyakan (75%) berjantina perempuan. Kejadian kembar siam banyak dilaporkan di A dan Afrika.
Istilah kembar siam berawal dari pasangan kembar siam terkenal Chang dan Eng Bunker (1811-1874) yang lahir di Siam (sekarang Thailand). Mereka mengembara bersama ahli sarkas P.T. Barnum selama bertahun-tahun dan popular dipanggil Kembar Siam. Kes kembar siam tertua yang tercatat adalah Mary dan Eliza Chulkhurst dari Inggeris yang lahir di tahun 1100-an

Penyebab kelahiran kembar

Banyak faktor diduga sebagai penyebab kehamilan kembar. Selain faktor genetik, ubat penyubur yang digunakan dengan tujuan agar sel telur matang secara sempurna, juga diduga ikut memicu terjadinya bayi kembar. Alasannya, jika indung telur boleh menghasilkan sel telur dan diberi ubat penyubur, maka sel telur yang matang pada saat bersamaan banyak, bahkan sampai lima dan enam.

Peratusan hidup

Sejumlah kesimpulan perubatan menyebutkan, terjadi satu kes kembar siam untuk setiap 200 ribu kelahiran. Dari semua kelahiran kembar siam, diyakni tidak lebih dari 12 pasangan kembar siam yang hidup di dunia. Saat dilahirkan kebanyakan kembar siam sudah dalam keadaan meninggal, yang lahir hidup hanya sekitar 40 peratus.
Dari mereka yang lahir hidup, 75 peratus meninggal pada hari-hari pertama dan hanya 25 peratus yang bertahan hidup. Itu pun sering kali disertai dengan kelainan bawaan dalam tubuhnya (incomplete conjoined twins). Apakah itu organ pada bagian ekstoderm, yakni kulit, hidung dan telinga atau mesoderm yang mencakup otot, tulang dan saraf atau juga indoderm, yakni bahagian organ dalam seperti hati, jantung, paru-paru dan otak.
Informasi Berbahasa Inggeris
The original siamese twins
No case history of conjoined twins can be complete without mention of the Bunker brothers, the original twins from Siam (present-day Thailand). Born on May 11, 1811 in a tiny village along the Mekong river, the brothers were xiphopagus twins, joined by only a small band of cartilage at the sternum. Their livers were fused but were each independently complete. Through practice they were able to stretch the tissue that connected them and stand side-by-side rather than facing one another. This gave the illusion that they were joined at the side, and even today conjoined twins are frequently depicted as joined side-by-side by a sliver of tissue. Separation of Chang and Eng would have been extremely easy, even with 19th century medical technology. Ironically, the boys were three-quarters Chinese and known in their native village as 'The Chinese Twins'.

At age 17, the boys were brought back to America by the showman Abel Coffin, whose associate had initially discovered them in 1824 while they were swimming. In America they toured with P.T. Barnum until their retirement in 1839. They adopted the last name Bunker in 1844, their original Siamese last names having been lost when they joined showbusiness. While in North Carolina, Chang and Eng began to date Adelaide and Sarah Ann (or Sally) Yates, respectively. They were scheduled to marry but locals disapproved strongly of the brothers' courtship of the girls and even threatened them. Fearing for their lives, the brothers arranged for a separation surgery, begging to be separated even if it meant killing them both. However, the sisters intervened just before the operation and married the twins in a quick double-wedding ceremony. One couple purchased a farm adjacent to the brothers' original property and the brothers built separate houses and raised tobacco. From then on, they spent alternating nights with their wives in their own houses and together fathered 22 children (10 were Chang's, 12 were Eng's). However, several of the children died in infancy or early childhood.

In 1874 Chang, the stronger and more stubborn of the twins and a heavy drinker, contracted pneumonia, which was worsened by the carriage trip in the rain between the two farms. He died rather suddenly during the night of January 17. Eng awoke to find his brother dead, and he called for his wife and children to attend to him. According to some stories, the family sent for a doctor to perform an emergency separation, but Eng had died by the time the doctor arrived. By other accounts, Eng refused to be separated from his dead brother. He died three hours later.

The twins' fused liver - the only organ the twins shared - is still preserved in formalin at the Mutter Museum in Philadelphia, Pennsylvania, and is exhibited alongside a plaster death-cast of the twins.


Conjoined twins occur in roughly 1 in every 200 identical twin pregnancies and are always identical. Actual numbers for conjoined births vary from 1 in 20,000 to 1 in 100,000 pregnancies, and 40-60% are stillborn, with many others dying within the first few days after birth. About 70% of conjoined twins are female, the reason for which is unknown.

Separation has been attempted on almost all conjoined twins born since the 1950s with varying results, although the first successful separation was performed in Basle, Switzerland in 1689 on twin girls born joined by a ligament at the sternum (xiphopagus). The first conjoined twins to be successfully separated in "modern" times are generally believed to be Catherine and Caroline Mouton of Louisiana, born joined at the lower back (pygopagus)and separated in 1953 at 8 days of age. Both survived the operation, but Catherine committed suicide in 1985.

Formation

There are two theories of how conjoined twins are formed. More widely accepted is the "fission theory" which states that conjoined twins occur when a fertilized ovum (egg) begins to split into identical twins, but is somehow interrupted during the process and develops into two partially formed individuals who are stuck together.

The "fusion theory" has been around much longer, but only with modern breakthroughs in understanding embryology has it begun to look more probable. According to this model, twins become conjoinedafter the fertilized ovum intially splits into identical twins. While lying side-by-side in the uterine wall, the two embryos become fused together. A human embryo, in its earliest stages, consists of three layers of cells. These cells "seek out" cells of the same type and thus bond together to form individual organs. When two newly-separated identical twin embryos are lying in close proximity to one another, sometimes signals get mixed and cells will attach to other cells of the same type, but that belong to the other twin.

The easiest example of the fusion theory to understand is the formation of craniopagus twins. One of the three "sheets" of tissue that comprises the embryo will ultimately "roll up" to become the neural tube - the spinal cord and brain. Like rolling a piece of paper into a tube and taping the edges, the edges of this newly-formed tube will adhere together. Spina bifida, a type of paralysis, is caused when these edges fail to join properly. For this to happen, the cells at the edges of the neural tube must be able to find and bond to one another. However, when two neural tubes are present, the cells at either end of the tubes might accidentally "find" each other, and become stuck.

This "fusion theory" of conjoined twinning has been espoused in recent years by such experts as Dr. Rowena Spencer, who has studied over 1,300 sets of conjoined twins in her 50-year career, and Armand Marie LeRoi, author of the book Mutants which discusses the embryological causes behind many of history's so-called "freaks".

Not surprisingly, the media tries to dumb down the science of conjoined twinning with such inaccurate phrases as "fused since birth" or "joined at birth" - making it seem as though conjoined twins are sort of forced into one body during the birthing process. Perhaps a more scientifically accurate description would be "joined since shortly after conception."

Types of conjoined twins

Conjoined twins are categorized by a set of adjectives ending with the suffix "-pagus" from the Greek word for "fixed". Early teratologists such as Ambroise Pare and Geoffrey St. Hillaire were among the first to identify and name the various types of conjoined twins. Many actual sets of twins do not fit perfectly into any of these classifications, and the terms are often combined to describe these twins.

Thoracopagus (left).

Joined at the upper chest, from the clavicle to the sternum, each with their own separate heads, arms and legs. The heart is always involved in the conjoinment; some thoracopagus twins have two separate hearts in a single pericardium (heart sac), while others share a single, malformed heart. Thus separation is extremely risky and both twins often die, despite doctors' efforts. In a very few cases, twins sharing a heart have survived for several years. Ruthie and Verena Cady of Rhode Island lived to the age of 7 and were healthy, active girls who rode a tricycle, swam, did gymnastics and went to school. Their shared heart had only 3 chambers. Thoracopagus twins are the most common type, accounting for around 35% of all cases.

Omphalopagus (right).

Joined at the abdomen, from the sternum to the groin and often sharing a liver and portions of the digestive system. These twins have separate hearts, heads, arms and legs. Separation is usually successful. Ronnie and Donnie Galyon, born in 1951, are the only non-separated omphalopagus twins in the world today. About 30% of cases.

Xiphopagus (left).

Joined at the xiphoid process (part of the sternum) and usually linked only by cartilage and soft tissue. These twins share no vital organs but often have conjoined livers. They are by far the easiest to separate. Chang and Eng Bunker (1811-1874) were xiphopagus twins with conjoined livers. Also called sternopagus. About 3% of cases.






Ischiopagus (right).

Joined at the ischium (front pelvis) and lower spine (sacrum), with spines at 180-degree angles to one another. These twins can have three legs (tripus) or four legs (tetrapus). About 70% of ischiopagus twins have four complete legs. In tripus cases, the third leg is a fusion of two legs that is not controlled by either twin and is therefore useless. Masha and Dasha Krivoshlyopova of Russia (1950-2003?) were ischiopagus tripus twins, their third leg having been removed when they were 16 years old. About 14% of cases.

Ischio-omphalopagus.

Combination of ischiopagus and omphalopagus, with spines joined in a "Y"-shape. These twins usually have three legs and a single set of genitalia.

Parapagus.

Joined side-by-side at the torso, having separate heads and arms and usually 3 legs. This is not a totally accurate term, since many of these twins are technically "xipho-thoraco-ischiopagus" or "xipho-omphalo-ischiopagus" or other long, cumbersome appellations.


Dicephalus (right).

A subset of parapagus. Twins share a body from the neck or upper chest downward, having only two legs and one set of reproductive organs. They can have two, three or four arms. If separate hearts are present, these twins have a good prognosis for long, healthy lives if not separated. Abigail and Brittany Hensel (1990- ) are healthy young girls who are dicephalus twins with two hearts. They love to play sports and are not at all limited by their conjoinment.



Craniopagus (left).

 Joined by a portion of the skull, with distinctly separate necks and bodies. Separation is very risky since these twins can share parts of the brain, as well as blood circulation. Craniopagus twins are further classified by the portion of the skull which is shared: vertical craniopagus - joined at the top of the head with bodies at a 180-degree angle to one another; occipital craniopagus - joined at the back of the head; frontal craniopagus - joined at the forehead; parietal craniopagus - joined at the side of the head.


Cephalopagus (right).

Twins with conjoined necks and heads but separate bodies. Due to malformations in the brain, these twins are never viable. Those that are not stillborn die within a few hours. Also called syncephalus or janiceps.



Cephalothoracopagus (left).

A combination of cephalopagus and thoracopagus. Twins with conjoined heads, necks and chests, with separate arms and legs. These usually share a heart as well as a brain and are also non-viable. Also called epholothoracopagus, prosopothoracopagus or craniothoracopagus.



Diprosopus.

Another subset of parapagus, describing a single organism with two faces on a single head. It is questionable whether some cases of diprosopus are even caused by twinning; however, if diprosopic babies are a form of conjoined twins, it would support a fission theory of conjoined twinning. This condition is rare in humans but relatively common in other animals such as sheep, cattle and cats. Gould & Pyle refer to this as "disprosopus" but I believe this to be a spelling error.

Pygopagus (right).

Joined back-to-back at the pelvis and lower spine, each with separate hearts, heads and limbs. Almost all pygopagus twins are female; most male twins of this type are stillborn. Historically, many pairs of conjoined twins who live to adulthood have been pygopagus. Separation is usually successful, although separating a conjoined spinal cord can lead to paralysis below the point of junction. Also called illeopagus.


Rachipagus (left).

Joined back-to-back at any point above the lumbar spine. Only one case of typical (non-parasitic) rachipagus twins has been recorded. These twins, reported in 1960, were joined from the mid-spine to the top of the head, with conjoined skulls. Rachipagus parasites are slightly more common, with approximately 20 cases reported (Spencer).

Parasitic twins.

Any of the above types can result in a case of parasitic twins if one twin dies or receives inadequate nutrition while in utero.

Acardiac twins.

An acardiac twin (acardiac meaning without a heart) is an incomplete fetus, usually consisting of a pair of legs, that shares the womb with a normal twin and is sustained by the twin's placenta. In other words, it is a parasitic twin that does not share a bodily connection with the normal twin.

Can conjoined triplets (or other higher multiples) exist?

Dr. Rowena Spencer's 2003 book Conjoined Twins: Developmental Malformations and Clinical Implications discusses several cases of supposed conjoined triplets and quadruplets, most of which consist of one autosite with a number of parasites or acardiac twins (see above). However, a 2004 article in The American Journal of Obstetrics and Gynecology describes a case of parapagus dicephalus dibrachius dipus twins with triplet joined to the shared sternum, in the manner of xiphopagus twins. All three fetuses were well-formed and had approximately normal heads and extremities. This article provides conclusive proof that conjoined triplets, although extremely uncommon, can occur.

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