منابع مشابه
Meckel-Gruber Syndrome with unilateral renal agenesis.
Meckel-Gruber Syndrome (MKS) is an autosomal recessive disorder, characterized by a combination of central nervous system malformation (occipital encephalocele), post-axial polydactyly, and enlarged polycystic kidney dysplasia. With a recurrence risk of 25% this lethal syndrome can be detected in early screening by ultrasound. However, to the authors' knowledge, association of MKS with unilater...
متن کاملUnilateral Renal Agenesis and the Awareness of Mostyn Embrey Syndrome
Background: Mostyn Embrey syndrome is a rare disorder associated with unilateral renal agenesis and malformations of the female reproductive tract. Delayed diagnosis is associated with serious diagnostic difficulties that may lead to inappropriate management including harmful surgery. Aim: The aim of this paper is to describe the first case of this rare syndrome in Iraq and, and to make a recom...
متن کاملKlippel-Feil syndrome with unilateral renal agenesis and renal failure.
Sir, T triad of short neck, low posterior hairline and severe restriction of cervical motion is a classic definition of KlippelFeil syndrome. Klippel-Feil syndrome (KFS) is characterized by congenital fusion of two or more cervical vertebrae and is believed to result from faulty segmentation along the embryo’s developing axis during the second to eighth week of gestation. This is commonly assoc...
متن کاملDoege-Potter syndrome
A male, 81-year-old patient admitted because of a progressive increase of the abdominal volume for five months, in association with daily episodes of sudden sweating with syncope. Physical examination revealed the presence of a palpable mass in the right flank and hypogastrium. Computed tomography (CT) (Figures 1A and 1B) demonstrated a voluminous, predominantly solid, expansile retroperitoneal...
متن کاملDoege–Potter syndrome
RATIONALE We reviewed 76 published cases of Doege-Potter syndrome, and non-islet cell tumor hypoglycemia (NICTH) secondary to a solitary fibrous tumor (SFT) between 1989 and 2016, to study disease pathogenesis, diagnosis, and treatment of this rare paraneoplastic disease. Further, we report 1 new case of a patient presenting with Doege-Potter syndrome. PATIENTS CONCERNS The tumors originated ...
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ژورنال
عنوان ژورنال: BMJ
سال: 1958
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.1.5079.1102