Journals / Journal of Clinical Research in Pediatric Endocrinology / 2016 / Cilt: 8 - Sayı: 1

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome

Pages
96–100
DOI
—
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AI Summary & Key Takeaways

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

Patients with NFNS who show poor growth should be evaluated for GHD.

📌 3 Key Takeaways

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Objective & Hypothesis:Neurofibromatosis-Noonan syndrome (NFNS) is a distinct entity which shows the features of both NF1 (neurofibromatosis 1) and Noonan syndrome (NS).
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Key Findings & Data:While growth hormone deficiency (GHD) has been relatively frequently identified in NF1 and NS patients, there is limited experience in NFNS cases.
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Conclusion & Impact:Patients with NFNS who show poor growth should be evaluated for GHD.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Neurofibromatosis-Noonan syndrome (NFNS) is a distinct entity which shows the features of both NF1 (neurofibromatosis 1) and Noonan syndrome (NS). While growth hormone deficiency (GHD) has been relatively frequently identified in NF1 and NS patients, there is limited experience in NFNS cases. The literature includes only one case report of a NFNS patient having GHD and that report primarily focuses on the dermatological lesions that accompany the syndrome and not on growth hormone (GH) treatment. Here, we present a 13-year-old girl who had clinical features of NFNS with a mutation in the NF1 gene. The case is the first NFNS patient reported in the literature who was diagnosed to have GHD and who received GH treatment until reaching final height. The findings in this patient show that short stature is a feature of NFNS and can be caused by GHD. Patients with NFNS who show poor growth should be evaluated for GHD.

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Cite This Article

KARAOĞLAN, D. V., GÖNÇ, E. N., VİDAUD, D., ÖZÖN, Z. A., ALİKAŞİFOĞLU, A., KANDEMİR, N. (2016). Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome. Journal of Clinical Research in Pediatric Endocrinology, Cilt: 8 - Sayı: 1, 96–100. https://ajindex.com/articles/216344

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