Cleidocranial dysplasia-A case report of incidentally found and lately diagnosed disorder.

Adhikari, Aayush; Shrestha, Suraj; Bhattarai, Prabin; Khanal, Surendra; Lamichhane, Rajan; Balayar, Ramesh; Panta, Sobin; Marasini, Kundan

Adhikari, Aayush; Shrestha, Suraj; Bhattarai, Prabin; Khanal, Surendra; Lamichhane, Rajan; Balayar, Ramesh; Panta, Sobin; Marasini, Kundan.

Afiliación

Adhikari A; Maharajung Medical Campus Institute of Medicine Kathmandu Nepal.
Shrestha S; Maharajung Medical Campus Institute of Medicine Kathmandu Nepal.
Bhattarai P; Department of Internal Medicine Tribhuvan University Teaching Hospital Kathmandu Nepal.
Khanal S; Maharajung Medical Campus Institute of Medicine Kathmandu Nepal.
Lamichhane R; Maharajung Medical Campus Institute of Medicine Kathmandu Nepal.
Balayar R; Maharajung Medical Campus Institute of Medicine Kathmandu Nepal.
Panta S; Maharajung Medical Campus Institute of Medicine Kathmandu Nepal.
Marasini K; Department of Radiology Tribhuvan University Teaching Hospital Kathmandu Nepal.

Clin Case Rep ; 10(10): e6440, 2022 Oct.

Article en En | MEDLINE | ID: mdl-36245444

Palabras clave

RUNX2; autosomal dominant; cleidocranial dysplasia

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Screening_studies Aspecto: Patient_preference Idioma: En Revista: Clin Case Rep Año: 2022 Tipo del documento: Article Pais de publicación: Reino Unido

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