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Family Multiple Pituitary Deficiencies Associated to Pituitary Process: Which Diagnosis?

Family Multiple Pituitary Deficiencies Associated to Pituitary Process: Which Diagnosis?

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1652208225

Family Multiple Pituitary Deficiencies Associated to Pituitary Process: Which Diagnosis?

About this item

Full title

Family Multiple Pituitary Deficiencies Associated to Pituitary Process: Which Diagnosis?

Publisher

Richmond: Sophia Publishing Group Inc

Journal title

International journal of clinical case reports, 2013-07, Vol.3 (11)

Language

English

Formats

Publication information

Publisher

Richmond: Sophia Publishing Group Inc

More information

Scope and Contents

Contents

The hypopituitarism of children, partial or absolute, stems from many causes. Tumor cause, such as craniopharyngioma, is predominant and must always be sought. The presence of a "tumor" pituitary lesion in a child with a GH deficiency, especially in family forms, should not overlook the possibility of a concomitant genetic disorder, in particular m...

Alternative Titles

Full title

Family Multiple Pituitary Deficiencies Associated to Pituitary Process: Which Diagnosis?

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_1652208225

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1652208225

Other Identifiers

ISSN

1927-579X

E-ISSN

1927-579X

DOI

10.5376/ijccr.2013.03.0011

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