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Journals / Türkiye Aile Hekimliği Dergisi / 2018 / Cilt: 22 - Sayı: 2

Presentation of Case of Aplasia Cutis Congenita Summary

Aplazia kutis konjenita: Olgu sunumu

Işık GÖNENÇ
Hatice DÜLEK
Güldehan ATIŞ
Zeynep Tuzcular VURAL
Pages
100–102
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

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

So we aim to remind in the differential diagnosis.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Aplasia cutis congenita (ACC) is a rare disease.
📊
Key Findings & Data:ACC is a disease characterized by absence of skin at birth.
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Conclusion & Impact:So we aim to remind in the differential diagnosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Aplasia cutis congenita (ACC) is a rare disease. ACC is a disease characterized by absence of skin at birth. Although associated with various syndromes, it is often seen as on isolated lesion. A five and a half month old boy with ACC was presented; it was observed that there was no scalp in the presence of the bone in this patient. Our country is an uncommon entity in the literature. So we aim to remind in the differential diagnosis.

Özet

Aplazia kutis konjenita (AKK) nadir görülen, doğumda cilt yokluğu ile karakterize bir hastalıktır. Çeşitli sendromlarla birlikteliği olsa da, genellikle izole lezyon olarak görülür. Burada kemik yokluğunun eşlik etmediği skalpte AKK tanısı alan beş buçuk aylık erkek çocuk sunulmuştur. Ülkemiz literatüründe seyrek rastlanan antiteyi ayırıcı tanıda hatırlatmayı amaçladık.

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Cite This Article

GÖNENÇ, I., DÜLEK, H., ATIŞ, G., VURAL, Z. T. (2022). Presentation of Case of Aplasia Cutis Congenita Summary. Türkiye Aile Hekimliği Dergisi, Cilt: 22 - Sayı: 2, 100–102. https://ajindex.com/articles/626678

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References (7)

  1. Bajpai M, Pal K. Aplasia cutis cerebri with partial acrania total re- construction in a severe case and review of the literature. J Pediatr Surg 2003;38(2):e4. Komuro Y, Yanai A, Seno H, et al. Surgical treatment of aplasia cutis congenita of the scalp associated with bilateral coronal syn- ostosis. J Craniofac Surg 2002;13:513-9.
  2. Moriya J, Kakeda S, Koragi Y. An unusual case of split cord mal- formation. Am J Neuroradiol 2006; 27,1562-4.
  3. Colon- Fontanez F, Fallon-Friedlander S, Newbury R, Eichen- field LF. Bullous aplasia cutis congenita. Am Acad Dermatol 2003;48:95-8. Frieden IJ. Aplasia cutis congenita: A clinical review and proposal for classification. J Am Acad Dermatol 1986;14:646-60.
  4. Garcia-Romero MT, Narvoez-Rosales V, Hojyo-tomoka MT. Bul- lous aplasia cutis congenita: Case report and review of the litera- ture. Indian J Dematol 2011;56:337-8.
  5. Sanchez-Pedreno Guillen P, Rodriguez-Pichardo A, Camo- cho- Martinez F. Aplasia cutis congenita. J Am Acad Dermatol 1985;13:429-33.
  6. Lane W, Zanol K. Duodenal atresia, biliary atresia, and intesti- nal infarct in truncal aplasia cutis congenita. Pediatr Dermatol 2000;17:290-2.
  7. Yapıcıoğlu H, Narlı N, Satar M, Erol A. Bir konjenital kutis aplasia olgusu. Türkiye Klinikleri Pediatri Dergisi 2000;9:240-2.