A Rare Variant of Turner Syndrome (the X Isochromosome-X Syndrome): A Case Report
Background: Turner syndrome occurs in nearly one in every 2000-5000 female births. This syndrome is a genetic problem in the female phenotype and the most common sex chromosome anomaly. It is diagnosed based on clinical manifestations and cytogenetic examinations. The classic syndrome (i.e., monosom...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Hormozgan University of Medical Sciences
2021-12-01
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| Series: | Disease and Diagnosis |
| Subjects: | |
| Online Access: | https://ddj.hums.ac.ir/PDF/ddj-10-177.pdf |