Pituitary Stalk Interruption Syndrome
Pituitary stalk interruption syndrome. Pituitary stalk interruption syndrome PSIS is a congenital disorder characterised by the triad of an absent or exceedingly thin pituitary stalk an ectopic or absent posterior pituitary andor absent or hypoplastic anterior pituitary. Pituitary stalk interruption syndrome PSIS is a congenital pituitary anatomical defect. Pituitary stalk interruption syndrome PSIS is a distinct and rare clinical entity responsible for congenital hypopituitarism resulting in deficiency of pituitary hormones with deficiency of the growth hormone 100 and gonadotropins 972 being its most common presentation at the time of hospital encounter Wang etal 2015.
Previous section General Endocrinology Table of contents Next section Reproductive and Developmental Endocrinology Pituitary stalk interruption syndrome. It can either present at birth or later in life. Pituitary stalk interruption syndrome is a congenital abnormality of the pituitary gland consisting of the triad of thin or interrupted pituitary stalk small or absent.
1 2 Signs and symptoms in newborns include low blood sugar levels hypoglycemia jaundice. We present a case of patient with post-trauma pituitary stalk transection resulting in. Pituitary stalk interruption syndrome also known as pituitary stalk transection syndrome is a syndrome characterized by an absent or hypoplastic anterior pituitary gland thin or absent infundibulum and ectopic posterior pituitary location.
The diagnosis of post-trauma pituitary stalk transection which is often life-threatening condition is frequently delayed. This syndrome is an antenatal developmental defect belonging to the holoprosencephaly phenotype spectrum. Mirica Alexandra Luiza Vitan Monica Preda Diana Loreta Paun Diana.
1 Spitalul Clinic de Urgenţă pentru Copii Grigore. A clinical case report. Pituitary stalk interruption syndrome PSIS is a congenital abnormality of the pituitary gland characterized by the triad of a very thin or interrupted pituitary stalk a misplaced ectopic or absent posterior pituitary and a small or absent anterior pituitary with permanent growth hormone GH deficit.
Pituitary and Neuroendocrinology. Pituitary stalk interruption syndrome PSIS is a rare congenital disorder characterized by a triad of a thin or interrupted pituitary stalk aplasia or hypoplasia of the anterior pituitary and absent or ectopic posterior pituitary EPP seen on magnetic resonance imaging MRI. Pituitary stalk interruption syndrome PSIS is a rare congenital disorder characterized by a triad of a thin or interrupted pituitary stalk aplasia or hypoplasia of the anterior pituitary and absent or ectopic posterior pituitary EPP seen on magnetic resonance imaging MRI.
It is heterogeneous regarding clinical biological and radiological presentation and is characterized by. In medical litera-ture still exist conflicting data concerning distinguishing this pathology with genetic developmental pituitary stalk interruption syndrome PSIS.
1 2 Signs and symptoms in newborns include low blood sugar levels hypoglycemia jaundice.
Pituitary stalk interruption syndrome PSIS is a rare congenital disorder characterized by a triad of a thin or interrupted pituitary stalk aplasia or hypoplasia of the anterior pituitary and absent or ectopic posterior pituitary EPP seen on magnetic resonance imaging MRI. 1 2 Signs and symptoms in newborns include low blood sugar levels hypoglycemia jaundice. Pituitary stalk interruption syndrome PSIS is a congenital pituitary anatomical defect. Pituitary stalk interruption syndrome also known as pituitary stalk transection syndrome is a syndrome characterized by an absent or hypoplastic anterior pituitary gland thin or absent infundibulum and ectopic posterior pituitary location. Pituitary stalk interruption syndrome is a congenital abnormality of the pituitary gland consisting of the triad of thin or interrupted pituitary stalk small or absent. Pituitary and Neuroendocrinology. A clinical case report. Previous section General Endocrinology Table of contents Next section Reproductive and Developmental Endocrinology Pituitary stalk interruption syndrome. This syndrome is an antenatal developmental defect belonging to the holoprosencephaly phenotype spectrum.
It is heterogeneous regarding clinical biological and radiological presentation and is characterized by. Pituitary stalk interruption syndrome PSIS is a rare congenital disorder characterized by a triad of a thin or interrupted pituitary stalk aplasia or hypoplasia of the anterior pituitary and absent or ectopic posterior pituitary EPP seen on magnetic resonance imaging MRI. A clinical case report. The diagnosis of post-trauma pituitary stalk transection which is often life-threatening condition is frequently delayed. It is heterogeneous regarding clinical biological and radiological presentation and is characterized by. We present a case of patient with post-trauma pituitary stalk transection resulting in. In medical litera-ture still exist conflicting data concerning distinguishing this pathology with genetic developmental pituitary stalk interruption syndrome PSIS.
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