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Neonatal osteoma cutis due to a mutation in GNAS.
Levy-Shraga, Yael; Barel, Ortal; Javasky, Elisheva; Barzilai, Aviv; Greenberger, Shoshana.
Afiliación
  • Levy-Shraga Y; Pediatric Endocrinology and Diabetes Unit, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat-Gan, Israel.
  • Barel O; The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Javasky E; The Genomic Unit, Sheba Cancer Research Center, Ramat-Gan, Israel.
  • Barzilai A; The Genomic Unit, Sheba Cancer Research Center, Ramat-Gan, Israel.
  • Greenberger S; The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Pediatr Dermatol ; 36(5): 732-734, 2019 Sep.
Article en En | MEDLINE | ID: mdl-31215057
We describe a 4-week-old baby boy who presented with white firm cutaneous nodules and failure to thrive. He did not have dysmorphic features, and laboratory tests including serum calcium, phosphorous, thyroid function, and parathyroid hormone level were within normal ranges. Whole exome sequencing revealed an inactivating mutation in GNAS that was previously described as causing pseudohypoparathyroidism.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cutáneas Genéticas / Enfermedades Óseas Metabólicas / Cromograninas / Osificación Heterotópica / Subunidades alfa de la Proteína de Unión al GTP Gs / Mutación Límite: Humans / Male / Newborn Idioma: En Revista: Pediatr Dermatol Año: 2019 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cutáneas Genéticas / Enfermedades Óseas Metabólicas / Cromograninas / Osificación Heterotópica / Subunidades alfa de la Proteína de Unión al GTP Gs / Mutación Límite: Humans / Male / Newborn Idioma: En Revista: Pediatr Dermatol Año: 2019 Tipo del documento: Article País de afiliación: Israel
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