Thanatophoric short stature is a rare genetic disorder that affects bone development in infants. It is characterized by extremely short limbs, a narrow chest, and poor lung development. This condition is usually diagnosed before birth or shortly after delivery.
Caused by a mutation in the FGFR3 gene, thanatophoric short stature affects the way bones grow and develop. The FGFR3 gene provides instructions for making a protein that is involved in the development and maintenance of bone and brain tissue. When this gene is mutated, it disrupts bone growth and leads to the characteristic features of the condition.
Symptoms of thanatophoric short stature:
It's important to note that thanatophoric short stature is a life-threatening condition. Infants born with this disorder often have severe respiratory complications, which can be fatal. Sadly, the majority of affected babies do not survive beyond a few days or weeks.
Diagnosing thanatophoric short stature typically involves prenatal ultrasound and genetic testing. During an ultrasound, the characteristic features of the condition, such as shortened limbs and narrow chest, may be observed. Genetic testing can confirm the presence of the FGFR3 gene mutation.
While there is no cure for thanatophoric short stature, supportive care is provided to manage the symptoms and improve the quality of life for affected infants. This may include respiratory support, physical therapy, and other interventions to address specific complications.
In conclusion, thanatophoric short stature is a rare genetic disorder that affects bone development in infants. It is characterized by severely shortened limbs, a narrow chest, and poor lung development. Early diagnosis is crucial for appropriate management and support. If you suspect your child may have this condition, consult a healthcare professional for further evaluation and guidance.
Thanatophoric short stature (TSS) is a severe skeletal disorder characterized by extremely short limbs and a narrow chest. This condition is caused by genetic mutations and affects bone development, leading to significant health challenges. While there is no cure for TSS, various treatment options can help manage the symptoms and im...
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