Ochoa syndrome: a spectrum of urofacial syndrome.

Ozgu Aydogdu; Berk Burgu; Fuat Demirel; Tarkan Soygur; Zeynep Birsin Ozcakar; Fatos Yalcınkaya; Serdar Tekgul

doi:10.1007/s00431-009-1042-9

Ochoa syndrome: a spectrum of urofacial syndrome.

Ozgu Aydogdu
, Berk Burgu
, Fuat Demirel
, Tarkan Soygur
, Zeynep Birsin Ozcakar
, Fatos Yalcınkaya
, Serdar Tekgul

Ankara University

Araştırma sonucu: Dergiye katkı › Makale › bilirkişi

24 Alıntılar (Scopus)

Özet

The urofacial syndrome, also known as Ochoa syndrome, is a rare autosomal recessive condition that occurs in both genders and characterized by uropathy and facial abnormalities. Early diagnosis is crucial for the management and prognosis of urinary problems due to a dysfunctional bladder. We report 11 patients with urofacial syndrome in five families from Turkey with a median follow up of 32 months (range, 2-44 months).

Orijinal dil	İngilizce
Sayfa (başlangıç-bitiş)	431-435
Sayfa sayısı	5
Dergi	European Journal of Pediatrics
Hacim	169
Basın numarası	4
DOI'lar	https://doi.org/10.1007/s00431-009-1042-9
Yayın durumu	Yayınlandı - Nis 2010
Harici olarak yayınlandı	Evet

Belgeye Erişim

10.1007/s00431-009-1042-9

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Bundan alıntı yap

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title = "Ochoa syndrome: a spectrum of urofacial syndrome.",

abstract = "The urofacial syndrome, also known as Ochoa syndrome, is a rare autosomal recessive condition that occurs in both genders and characterized by uropathy and facial abnormalities. Early diagnosis is crucial for the management and prognosis of urinary problems due to a dysfunctional bladder. We report 11 patients with urofacial syndrome in five families from Turkey with a median follow up of 32 months (range, 2-44 months).",

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TY - JOUR

T1 - Ochoa syndrome

T2 - a spectrum of urofacial syndrome.

AU - Aydogdu, Ozgu

AU - Burgu, Berk

AU - Demirel, Fuat

AU - Soygur, Tarkan

AU - Ozcakar, Zeynep Birsin

AU - Yalcınkaya, Fatos

AU - Tekgul, Serdar

PY - 2010/4

Y1 - 2010/4

N2 - The urofacial syndrome, also known as Ochoa syndrome, is a rare autosomal recessive condition that occurs in both genders and characterized by uropathy and facial abnormalities. Early diagnosis is crucial for the management and prognosis of urinary problems due to a dysfunctional bladder. We report 11 patients with urofacial syndrome in five families from Turkey with a median follow up of 32 months (range, 2-44 months).

AB - The urofacial syndrome, also known as Ochoa syndrome, is a rare autosomal recessive condition that occurs in both genders and characterized by uropathy and facial abnormalities. Early diagnosis is crucial for the management and prognosis of urinary problems due to a dysfunctional bladder. We report 11 patients with urofacial syndrome in five families from Turkey with a median follow up of 32 months (range, 2-44 months).

UR - https://www.scopus.com/pages/publications/77952519873

U2 - 10.1007/s00431-009-1042-9

DO - 10.1007/s00431-009-1042-9

M3 - Article

C2 - 19669792

AN - SCOPUS:77952519873

SN - 0340-6199

VL - 169

SP - 431

EP - 435

JO - European Journal of Pediatrics

JF - European Journal of Pediatrics

IS - 4

ER -

Ochoa syndrome: a spectrum of urofacial syndrome.

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