Results 151 to 160 of about 3,689 (193)

Congenital hypopituitarism: clinical, molecular and neuroradiological correlates

Clinical Endocrinology, 2009
SummaryObjective  Recent studies have suggested that mutations in genes encoding several hypothalamo–pituitary (H–P) transcription factors result in hypopituitarism [isolated GH deficiency (IGHD) and combined pituitary hormone deficiency (CPHD)], which may in turn be related to the neuroanatomy revealed by magnetic resonance (MR) imaging.
Ameeta, Mehta, Peter C, Hindmarsh, Hiten, Mehta, James P G, Turton, Isabelle, Russell-Eggitt, David, Taylor, W K, Chong, Mehul T, Dattani   +7 more
openaire   +2 more sources

Sensorineural Deafness in Congenital Hypopituitarism with Severe Hypothyroidism

Acta Paediatrica, 1985
ABSTRACT. Marked sensorineural hearing loss was documented in an 18‐year‐old boy with untreated congenital anterior panhypopituitarism. The clinical manifestations of the hypothalamic thyroid failure were unusually severe in this patient. Seemingly this is the first case report of perceptive‐cochlear deafness in a subject with non primary congenital ...
DE LUCA, Filippo, ARRIGO, Teresa, Mangione OA, Maiolino MG, Muritano M.   +4 more
openaire   +3 more sources

Congenital Hypopituitarism and Conjugated Hyperbilirubinemia in Two Infants

Archives of Pediatrics & Adolescent Medicine, 1978
Congenital hypopituitarism in children is a well-recognized entity. 1-10 The association of severe neonatal hypoglycemia with growth hormone or adrenocorticotropin insufficiency and with the presence of a microphallus and cryptorchidism in some of the male patients is well established.
R, Lanes, V, Blanchette, C, Edwin, K, Zahka, P A, Lee, L C, Pakula, W C, MacLean, L P, Plotnick   +7 more
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Congenital hypopituitarism and microphthalmia. Report of two cases

Acta Paediatrica, 1993
Two children are described who had microphthalmia (one with unilateral and one with bilateral) noted at birth, and whose early onset of poor linear growth and weight gain led to a diagnosis of hypopituitarism prior to two years of age. Both children had growth hormone and thyroid‐stimulating hormone deficiencies, and evidence of partial ACTH deficiency.
P B, Kaplowitz, J, Bodurtha
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Familial congenital hypopituitarism with central diabetes insipidus.

The Journal of Clinical Endocrinology & Metabolism, 1994
Congenital hypopituitarism (CH) presenting with central diabetes insipidus is typically associated with midline facial deformities or ophthalmological abnormalities. We present three brothers with CH and central diabetes insipidus not associated with any of these predisposing conditions.
H, Yagi, K, Nagashima, H, Miyake, S, Tamai, K, Onigata, S, Yutani, T, Kuroume   +6 more
openaire   +3 more sources

Congenital Hypopituitarism in Female Infants

American Journal of Diseases of Children, 1979
Congenital hypopituitarism was found in two female infants who had profound hypoglycemia and hypothyroidism. In both infants, death occurred despite recognition of the disorder and institution of appropriate therapy. Autopsy findings showed an absent pituitary gland and sella turcica, with hypoplastic adrenal and thyroid glands, and ovaries in one case,
A, Kauschansky, M, Genel, G J, Smith
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Galactocele in a Male Infant with Congenital Hypopituitarism

Journal of Pediatric Endocrinology and Metabolism, 2004
Galactocele is an uncommon benign breast lesion usually occurring in young lactating women. It is a rare cause of breast enlargement in children. We report a galactocele in a male child with congenital hypopituitarism and propose an association between the two conditions.
N, Rahman, M, Davenport, C, Buchanan
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Optic nerve hypoplasia and congenital hypopituitarism

Journal of Pediatrics, 2000
M C, Brodsky, P H, Phillips
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Neonatal Cholestasis, Hypoglycemia, and Congenital Hypopituitarism

Journal of Pediatric Gastroenterology and Nutrition, 1992
A G, Sheehan, S R, Martin, D, Stephure, R B, Scott   +3 more
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Undetectable adrenal glands in neonates indicate congenital hypopituitarism

Pediatrics International, 2022
Dai Kataoka, Sota Iwatani, Akari Mitsuboshi, Kayo Ozaki, Seiji Yoshimoto   +4 more
openaire   +2 more sources