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Syndromes / 22q13 deletion syndrome / Pediatrics / Chromosome 22 / Diabetes insipidus / DiGeorge syndrome / Deletion / Neurogenic diabetes insipidus / Diabetes / Health / Genetics / Biology


Document Date: 2005-07-13 11:12:52

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City

Washington / /

Company

Wilson / CDI / /

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Facility

Georgetown University Medical Center / National Medical Center / bGeorge Washington University / /

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MedicalCondition

polyuria / Persistent central diabetes insipidus / reversible central diabetes insipidus / genetic disease / central hypotonia / disease / autistic syndrome / diabetes insipidus / hypotonia / normal growth / Autism / dominant neurohypophyseal diabetes insipidus / severe expressive language delay / mild mental retardation / 22q13 Deletion Syndrome / persistent deficiency / panhypopituitarism / deletion syndrome / Transient diabetes insipidus / generalized hypotonia / hypotonia / speech delay / deficiency / Central Diabetes Insipidus / syndrome / terminal 22q13 deletion syndrome / pervasive developmental disorders / /

Organization

D.C and cChildren’s National Medical Center Washington / Georgetown University Medical Center / Washington University / Previously Unreported Association / /

Person

Ashok Gr / Phillip L. Pearlb / Raji Op / Arch Fr Pediatr / Maria T. Acostac / Beatriz P. Runklea / Xue Za Zhi / Amin J. Barakata / Amin J. Barakat / /

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Position

AUTHOR / Professor of Pediatrics / /

Product

DDAVP / /

ProvinceOrState

Washington / /

PublishedMedium

Lippincott Williams & Wilkins / /

Region

North Virginia / /

Technology

hybridization / ultrasound / MRI / /

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