Williams syndrome

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Williams syndrome


Genetic disorders


Alagille syndrome (NORD)

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Huntington disease

Li-Fraumeni syndrome

Marfan syndrome

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Sickle cell disease (NORD)

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Cri du chat syndrome

Williams syndrome

Angelman syndrome

Prader-Willi syndrome

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Mitochondrial myopathy

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Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)

Muscular dystrophy

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X-linked agammaglobulinemia

Autosomal trisomies: Pathology review

Miscellaneous genetic disorders: Pathology review

Muscular dystrophies and mitochondrial myopathies: Pathology review


Williams syndrome


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Williams syndrome

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USMLE® Step 1 style questions USMLE

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A 2-year-old boy is brought to the pediatrician by his parent for a routine checkup. His parent describes him as very friendly, even with strangers. The patient’s growth was slow in the first year of life, where he was placed in the 3rd percentile for weight. His weight improved with a special formula, and he is currently at the 10th percentile for weight. The child was also discovered to have supravalvular aortic stenosis at two months. Physical examination demonstrates a child with a broad nasal bridge, wide forehead, and upturned nose. The child is extremely friendly with the physician. Labs demonstrate hypercalcemia. Which of the following is most likely the disease mechanism in this patient?  

External References

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Aortic stenosis

Williams syndrome p. 306

Hypercalcemia p. 615

Williams syndrome p. 62

Williams syndrome p. 62

cardiac defect association p. 306


Content Reviewers


Williams syndrome, also known as Williams-Beuren syndrome, is named after Dr. J. C. P. Williams who first described it.

This is a chromosome disorder in which a small portion of chromosome 7 is deleted, which results in physical and developmental problems.

Now, our DNA is this humongous blueprint on how to make a human and it’s usually packaged up nicely into 46 chromosomes.

These 46 chromosomes come in 23 pairs - and each pair has one chromosome from each parent.

Now, the individual chromosomes are shaped like an “X” with two short arms and two long arms linked together in the center by a centromere.

These two short arms are also referred to as p arms from the French term “petit” meaning small.

What's more, the two long arms are also referred to as q arms, since 'q' follows 'p' in the alphabet.

In Williams syndrome, about 26 to 28 genes, including the elastin gene (ELN) on the long arm of chromosome 7 are missing due to a microdeletion.

In most cases, this occurs randomly during the formation of sex cells in one of the parents.

So a sperm cell or an ovum can potentially carry this microdeletion on the long arm of its chromosome 7 and go on to fuse with another sex cell - forming a new organism which has the microdeletion.

Rarely, the cause of Williams syndrome can also be inherited in an autosomal dominant fashion - so when a person with Williams syndrome has children, there is a 50% chance they’ll pass down their own microdeletion to the offspring.

Now, the precise location of the microdeletion is at band 7q11.23, just like the directions to an address: 7 stands for chromosome 7, 'q' refers to the long arm, 11.23 refers to the specific region on the chromosome- and then it gets very specific: region 1, band 1, sub-band 2, sub-sub-band 3.

This section of DNA spans about 26 to 28 genes and 1.5 to 1.8 million base pairs - so this is considered a microdeletion, because we’re talking about less than 5 million base pairs.

Even though this region is pretty small, it codes for some very important genes, one of which is the elastin gene, which is responsible for the production of elastin protein which allows many tissues in the body to resume their shape after stretching or contracting.

So the symptoms of Williams syndrome are linked to connective tissue abnormalities resulting from these missing genes.

For example, the loss of the elastin gene leads to a broad forehead, flat nasal bridge, periorbital puffiness, short upturned nose, long medial cleft, full lips, and wide mouth that in combination give an "elfin" like appearance.


Williams syndrome is a chromosome disorder that results from the deletion of certain genes, including the elastin gene, on the long arm of chromosome 7. This leads to physical and developmental problems, such as a unique "elfin" facial appearance, cognitive impairment, weak visual motor and visual-spatial abilities, and hypercalcemia. The syndrome is suspected by clinical features and can be confirmed with microarray analysis or fluorescence in situ hybridization (FISH). There is no cure for Williams syndrome, and management involves treating associated conditions such as congenital heart defects, hypertension, and hypercalcemia, and providing therapy to maximize development and independence.


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