Results 221 to 230 of about 5,557 (240)

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   +4 more sources

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
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.
Lawrence C. Pakula, Victor Blanchette, Leslie P. Plotnick, Kenneth G. Zahka, Chandra Edwin, Peter A. Lee, Roberto Lanes, William C. MacLean   +7 more
openaire   +3 more sources

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, Wui K. Chong, Hiten Mehta, Peter C. Hindmarsh, Mehul T. Dattani, David Taylor, Isabelle Russell-Eggitt, James P. G. Turton   +7 more
openaire   +3 more sources

Congenital hypopituitarism presenting as dilated cardiomyopathy in a child

Journal of Pediatric Endocrinology and Metabolism, 2011
Congenital hypopituitarism is commonly diagnosed either in infancy with neonatal hypoglycemia, prolonged jaundice and/or microphallus or in early to mid-childhood because of short stature. Replacement of deficient hormones allows the affected children to have a normal and productive life.
Pawan Kumar, Lakshminarayanan Kannan, Vandana Jain   +2 more
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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.
Kazumichi Onigata, Takayoshi Kuroume, Hideki Yagi, Shinya Tamai, Hiroshi Miyake, Kanji Nagashima, Shigenori Yutani   +6 more
openaire   +2 more sources

[Cholestatic hepatopathy in a child with congenital hypopituitarism].

Pediatrie, 1986
The present case report concerns a male infant affected by congenital hypopituitarism presenting with neonatal hypoglycaemic attacks, microphallus and bilateral cryptorchidism. A transient cholestasis observed during the 2nd month of life and reversed by hydrocortisone treatment, is to be considered, in Authors' opinion, in the context of the endocrine
DE LUCA, Filippo, Pandullo E, Polimeni A, Sindoni A, Gemelli M.   +4 more
openaire   +2 more sources

Neonatal hypoglycemia caused by hypopituitarism in infants with congenital syphilis

The Journal of Pediatrics, 1993
Two infants with congenital syphilis and persistent hypoglycemia were found to have hypopituitarism. Hypopituitarism should be recognized as a potential complication of congenital syphilis; affected infants with persistent hypoglycemia should receive a prompt evaluation of pituitary function.
Jorge Daaboul, Kenneth Lee Jones, Kenneth Lee Jones, Wade Kartchner, Wade Kartchner   +4 more
openaire   +2 more sources

Optic nerve hypoplasia and congenital hypopituitarism

Journal of Pediatrics, 2000
Paul H. Phillips, Michael C. Brodsky
openaire   +3 more sources

Growing heart in congenital hypopituitarism treated in adulthood

The Lancet, 2023
Fromes, Yves, Chasseloup, Fanny, Bouvattier, Claire, Creze, Maud, Trabado, Séverine, Young, Jacques, Chanson, Philippe, Marty, Benjamin, Kamenický, Peter   +8 more
openaire   +3 more sources