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Sindrom Turner

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Turner syndrome is a congenital disorder, due to partial or total loss of X chromosome (45, XO). The defmitive etiology is unknown. The incidence is 2.5- 5.5 per 10.000 female live birth. Diagnosis could be established since intrauterine period to birth. The intrauterine diagnosis could be established by applying USG, amniocentesis, and by measuring the alpha feto protein level.'-4 At birth, diagnosis could be established by physical characteristic examination and chromosome analysis. This paper reports two cases of Turner syndrome diagnosed antenatally at the Obstetric and Ginecology's clinic, FK. UK! Hospital, Jakarta.

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Ketersediaan

Informasi Detail

Judul Seri

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No. Panggil

Majalah fk. Universitas Kristen Indonesia;27(1)201

Penerbit

Jakarta : FK Universitas Kristen Indonesia., 2010

Deskripsi Fisik

4p.

Bahasa

ISBN/ISSN

0216-4752

Klasifikasi

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Tipe Isi

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Tipe Media

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Tipe Pembawa

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Edisi

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Subjek

TURNER SYNDROME
CONGENITAL, HEREDITARY, AND NEONATAL DISEASE AND A

Info Detail Spesifik

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Pernyataan Tanggungjawab

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Versi lain/terkait

Lampiran Berkas

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