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Journals / The Journal of Pediatric Research / 2018 / Cilt: 5 - Sayı: 2

Triple X Syndrome with a Rare Finding: Cleft Palate

Esra GÜRKAŞ
Hülya MARAŞ GENÇ
ESRA KILIÇ
Pages
100–102
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

By describing this case, we want to draw attention to the association between cleft palateand Triple X syndrome.

📌 3 Key Takeaways

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Objective & Hypothesis:Triple X syndrome (trisomy X) is a sex chromosomal anomaly caused by the presence of an extra X chromosome.
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Key Findings & Data:The patients with Triple X syndromehave a wide range of phenotypic variability.
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Conclusion & Impact:By describing this case, we want to draw attention to the association between cleft palateand Triple X syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Triple X syndrome (trisomy X) is a sex chromosomal anomaly caused by the presence of an extra X chromosome. The patients with Triple X syndromehave a wide range of phenotypic variability. Some individuals are only mildly affected or asymptomatic. Epicanthal folds, clinodactyly, tall stature andhypotonia are the most commom phenotypic features. Patients also may have seizures, genitourinary abnormalities and premature ovarian failure.We report a patient with Triple X syndrome and cleft palate. By describing this case, we want to draw attention to the association between cleft palateand Triple X syndrome.

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Cite This Article

GÜRKAŞ, E., GENÇ, H. M., KILIÇ, E. (2018). Triple X Syndrome with a Rare Finding: Cleft Palate. The Journal of Pediatric Research, Cilt: 5 - Sayı: 2, 100–102. https://ajindex.com/articles/362914

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References (8)

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