Your browser doesn't support javascript.
loading
PLACK syndrome is potentially treatable with intralipids.
Sawan, Zinab A; Almehaidib, Ali; Binamer, Yousef; Monies, Dorota; Alsaleem, Khalid A; Aldekhail, Wajeeh; Alkuraya, Fowzan S; Abanemai, Mohammed.
Afiliación
  • Sawan ZA; Department of Pediatrics, King Abduaziz University, Faculty of Medicine, Jeddah, Kingdom of Saudi Arabia.
  • Almehaidib A; Department of Pediatrics, Division of Gastroenterology, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
  • Binamer Y; Department of Pediatrics, Division of Gastroenterology, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
  • Monies D; Department of Dermatology, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
  • Alsaleem KA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
  • Aldekhail W; Saudi Human Genome Program, King Abdul-Aziz City for Science and Technology, Riyadh, Kingdom of Saudi Arabia.
  • Alkuraya FS; Department of Pediatrics, Division of Gastroenterology, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
  • Abanemai M; Department of Pediatrics, Division of Gastroenterology, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
Clin Genet ; 99(4): 572-576, 2021 04.
Article en En | MEDLINE | ID: mdl-33410500

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fosfolípidos / Enfermedades Cutáneas Genéticas / Aceite de Soja / Hipopigmentación / Dermatitis Exfoliativa / Enfermedades de la Uña Tipo de estudio: Etiology_studies Límite: Child / Female / Humans Idioma: En Revista: Clin Genet Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fosfolípidos / Enfermedades Cutáneas Genéticas / Aceite de Soja / Hipopigmentación / Dermatitis Exfoliativa / Enfermedades de la Uña Tipo de estudio: Etiology_studies Límite: Child / Female / Humans Idioma: En Revista: Clin Genet Año: 2021 Tipo del documento: Article