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