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Van Wyk Grumbach Syndrome.
Riaz, Maira; Ibrahim, Mohsina Noor; Laghari, Taj Muhammad; Hanif, Misbah Iqbal; Raza, Jamal.
Afiliação
  • Riaz M; Department of Paediatrics, National Institute of Child Health, Karachi, Pakistan.
  • Ibrahim MN; Department of Paediatrics, National Institute of Child Health, Karachi, Pakistan.
  • Laghari TM; Department of Paediatrics, National Institute of Child Health, Karachi, Pakistan.
  • Hanif MI; Department of Paediatrics, National Institute of Child Health, Karachi, Pakistan.
  • Raza J; Department of Paediatrics, National Institute of Child Health, Karachi, Pakistan.
J Coll Physicians Surg Pak ; 30(12): 1332-1334, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33397063
ABSTRACT
Van Wyk Grumbach syndrome is well known for protracted hypothyroidism, characterised by multicystic ovaries (normal size ovaries contain many follicles of various sizes), isosexual precocious puberty and delayed skeletal growth. A series of ten children with Van Wyk Grumbach syndrome is been presented with their clinical features, biochemical and radiological profile and management. Patients showed a noteworthy improvement upon thyroxine therapy. It is vital to keep this entity in consideration and; hence, should investigate for thyroid status during the evaluation of ovarian cysts. Thyroxin replacement after establishing the diagnosis early can prevent the patient from going through extensive workup and surgeries. Key Words Hypothyrodism, Multicystic ovaries, Isosexual precocious puberty.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cistos Ovarianos / Síndrome do Ovário Policístico / Puberdade Precoce / Hipotireoidismo Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cistos Ovarianos / Síndrome do Ovário Policístico / Puberdade Precoce / Hipotireoidismo Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article