Journals / Türkiye Çocuk Hastalıkları Dergisi / 2011 / Cilt: 5 - Sayı: 2

A HYPOMELANOSIS ITO PATIENT PRESENTING WITH NEONATAL MACROCEPHALY

Neonatal Makrosefali ile Başvuran Bir Hipomelanozis Ito Olgusu

Pages
104–107
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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

We report a newborn case presenting with macrocephaly after than diagnosed as hypomelanosis of Ito

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Macrocephaly is defined as a head circumference that exceeds the mean by more than two standard deviations or is above the 98th percentile.
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Key Findings & Data:Except familial ones, macrocephaly frequently has been associated with various degrees of neurological dysfunction.
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Conclusion & Impact:We report a newborn case presenting with macrocephaly after than diagnosed as hypomelanosis of Ito
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Makrosefali · yenidoğan · hipomelanozis Ito

Abstract

Macrocephaly is defined as a head circumference that exceeds the mean by more than two standard deviations or is above the 98th percentile. Except familial ones, macrocephaly frequently has been associated with various degrees of neurological dysfunction. Hypomelanosis of Ito is a neurocutaneous disorder characterized by unilateral or bilateral macular hypopigmented whorls, streaks and patches. Abnormalities of the central nervous system and musculoskletal system may also be present in more than half of the cases. We report a newborn case presenting with macrocephaly after than diagnosed as hypomelanosis of Ito

Özet

Makrosefali baş çevresinin ortalamanın iki standart sapma veya 98 persentil üzerinde olmasıdır. Ailesel olgular hariç makrosefali genellikle çeşitli derecelerde nörolojik işlev bozukluğu ile birliktedir. Hipomelanosis Ito tek taraflı veya iki taraflı halkasal, çizgisel veya yama tarzında hipopigmente lekelerle kendini gösteren bir nörokütanöz bozukluktur. Hastaların yarıdan fazlasında nörolojik ve kas-iskelet sistemi tutulumu bulunur. Bu yazıda yenidoğan döneminde makrosefali ile başvuran ve takiplerinde hipomelanozis Ito tanısı alan bir olgu sunuldu.

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Cite This Article

DEĞERLİYURT, A., ŞENKON, G., TANRIKULU, B., İNÖZÜ, M. (2022). A HYPOMELANOSIS ITO PATIENT PRESENTING WITH NEONATAL MACROCEPHALY. Türkiye Çocuk Hastalıkları Dergisi, Cilt: 5 - Sayı: 2, 104–107. https://ajindex.com/articles/627626

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References (4)

  1. DeMyer William. Megalencephaly: types, clinical syndromes, and management. Pediatr Neurol 1986;2(6):321-8. Olney AH. Macrocephaly syndromes. Semin Pediatr Neurol 2007;14(3):128-35.
  2. Pascual-Castroviejo I, Lopez-Rodriguez L, de la Cruz Medina M, Salamanca-Maesso C, Roche Herrero C. Hypomelanosis of Ito. Neurological complications in 34 cases. Can J Neurol Sci 1988;15(2):124-9.
  3. Nevo Y, Kramer U, Shinnar S, Leitner Y, Fattal-Valevski A, Villa Y, et al. Macrocephaly in children with developmental disabilities. Pediatr Neurol 2002;27(5):363-8.
  4. Williams CA, Dagli A, Battaglia A. Genetic disorders associated with macrocephaly. Am J Med Genet Part A 2008;146A(15):2023- 37. Courchesne E, Carper R, Akshoomoff N. Evidence of brain over- growth in the first year of life in autism. JAMA 2003;290(3):337- 44. Pascual-Castroviejo I, Roche C, Martinez-Bermejo A, Arcas J, Lo- pez-Martin V, Tendero A, et al. Hypomelanosis of ITO. A study of 76 infantile cases. Brain Dev 1998;20(1):36-43. Gordon N. Hypomelanosis of Ito (Incontinentia pigmenti achromi- ans). Dev Med Child Neurol 1994; 36(3):271-4. Araknoid kistler