Triploid syndrome

{{short description|Chromosomal disorder in which there are three copies of every chromosome}}

{{Infobox medical condition (new)

| synonyms = 69,XXX{{cite journal |vauthors=Erol O, Erol M, Karaca M |title=Complete chorioamniotic separation and persistence of a yolk sac associated with triploidy |journal=Journal of Obstetrics and Gynaecology Canada |volume=35 |issue=10 |pages=914–6 | date=October 2013 |pmid=24165059|doi=10.1016/S1701-2163(15)30813-6 |doi-access=free }} 2n/3n mixoploidy, 3n syndrome, chromosome triploidy syndrome, diploid/triploid mixoploidy, triploidy, triploidy syndrome

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|alt=| caption = A karyotype of a person with triploidy

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Triploid syndrome, also called triploidy, is a chromosomal disorder in which a fetus has three copies of every chromosome instead of the normal two. If this occurs in only some cells, it is called mosaic triploidy and is less severe.

Most embryos with triploidy miscarry early in development.

Signs and symptoms

Many organ systems are affected by triploidy, but the central nervous system and skeleton are the most severely affected:

Common central nervous system defects seen in triploidy include holoprosencephaly, hydrocephalus (increased amount of cerebrospinal fluid within the brain), ventriculomegaly, Arnold–Chiari malformation, agenesis of the corpus callosum and neural tube defects.{{cn|date=November 2020}}

Skeletal manifestations include cleft lip/palate, hypertelorism, club foot and syndactyly of fingers three and four{{cn|date=November 2020}}.

Congenital heart defects, hydronephrosis, omphalocele and meningocele (spina bifida) are also common. Cystic hygromas occur but are uncommon.{{cn|date=November 2020}}

Triploid fetuses have intrauterine growth restriction beginning early in the pregnancy, as early as 12 weeks, and does not affect the head as severely as the body. Oligohydramnios, low levels of amniotic fluid, is common in triploid pregnancies. Placental abnormalities are common in triploidy. Most frequently, the placenta is enlarged and may have cysts within. In some cases, the placenta may be unusually small, having ceased to grow.{{Cite book|url=https://books.google.com/books?id=GeBsAAAAMAAJ|title=Structural Fetal Abnormalities: The Total Picture|last=Sanders|first=Roger C.|date=2002-01-01|publisher=Mosby|isbn=9780323014762|language=en}}

During the first trimester, fetuses with triploidy have a thicker fluid under the skin behind their neck, which calls for observation during the first and second trimester of gestation.{{cn|date=September 2020}}

The mother will usually have high levels of specific proteins including maternal serum alpha-fetoprotein (AFP) and beta-human chorionic gonadotropin (hCG). Symptoms may include, but are not limited to, swelling, edema, or hypertension.{{medical citation needed|date=July 2023}}

Infants may show facial abnormalities, micrognathia, cleft lip, spina bifida, as well as other birth defects that result from kidney, limb, and umbilical cord complications. They are also prone to being smaller than a normal sized newborn, a problem that arises while the infant is still a fetus.{{cn|date=September 2020}}

Causes

Triploidy is caused by an extra set of chromosomes.{{cn|date=August 2021}}

Triploidy can result from either two sperm fertilizing one egg (polyspermy) (60%) or from one sperm fertilizing an egg with two copies of every chromosome (40%). These are otherwise known as diandric fertilization and digynic fertilization. Pregnancies caused by digynic fertilization are more likely to end right before a baby is due for full term. Pregnancies caused by diandric fertilization result in a miscarriage towards the first trimester.{{medical citation needed|date=July 2023}}

Another factor known as a partial mole pregnancy can cause triploidy. It is known to cause early termination, cancer, and even a second molar pregnancy.{{medical citation needed|date=July 2023}}

Diagnosis

Triploidy may be suggested by dramatically elevated levels of serum alpha-fetoprotein. On obstetric ultrasonography, abnormalities of the skeleton, central nervous system, heart, abdomen, and kidneys are visible in the most severe cases beginning at 12-14 weeks of pregnancy. Placental abnormalities associated with a triploid pregnancy become visible at 12-14 weeks. Placentomegaly or intrauterine growth restriction are the typical findings that prompt evaluation for triploidy, though oligohydramnios may be the first sign in some cases. Placentomegaly is not pathognomonic for triploidy because in some cases, the placenta senesces.

Triploidy must be distinguished from trisomy 13 and trisomy 18, which may appear similar on sonography. Genetic testing allows for a definitive diagnosis.

A sample of amniotic fluid can also be tested to diagnose triploidy.{{medical citation needed|date=July 2023}}

Prognosis

Most fetuses with triploidy do not survive to birth, and those that do usually die within days. As there is no treatment for triploidy, palliative care is given if a baby survives to birth. If triploidy is diagnosed during the pregnancy, termination is often offered as an option due to the additional health risks for the mother (pre-eclampsia, a life-threatening condition, or choriocarcinoma, a type of cancer). Should a mother decide to carry until term or until a spontaneous miscarriage occurs, doctors will monitor her closely in case either condition develops.{{cn|date=November 2020}}

Mosaic triploidy has an improved prognosis, but affected individuals have moderate to severe cognitive disabilities.

Epidemiology

Triploidy affects approximately 1–2% of pregnancies, but most miscarry early in development. At birth, males with triploidy are 1.5 times more common than females.