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Combination of four features of SLC29A3 spectrum disorder in a child: A case report.
Aslani, Nahid; Abtahi-Naeini, Bahareh; Rastegarnasab, Fereshte; Derakhshan, Maryam; Tavousi, Elham; Mehraein, Kimia.
Afiliação
  • Aslani N; Pediatric Rheumatology Society of Iran, Tehran, Iran.
  • Abtahi-Naeini B; Department of Pediatrics, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Rastegarnasab F; Pediatric Dermatology Division of Department of Pediatrics, Imam Hossein Children's Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Derakhshan M; Skin Diseases and Leishmaniasis Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Tavousi E; Student Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Mehraein K; Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Pediatr Dermatol ; 2024 Apr 30.
Article em En | MEDLINE | ID: mdl-38689526
ABSTRACT
SLC29A3 spectrum disorder, also known as histiocytosis-lymphadenopathy plus syndrome (HLPS), presents a wide variety of multi-systemic manifestations that can be mistaken for other conditions. Herein, we report a 9-year-old girl who presented with a complex clinical presentation since birth, including chronic generalized lymphadenopathy in association with hepatosplenomegaly, short stature, flexion contractures, hearing loss, hyperpigmentation, and heart anomalies. She was ultimately diagnosed with the SLC29A3 spectrum disorder.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pediatr Dermatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pediatr Dermatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Irã