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Hereditary osteodystrophy with multiple hormone resistance--a case report.

Identifieur interne : 000362 ( Main/Exploration ); précédent : 000361; suivant : 000363

Hereditary osteodystrophy with multiple hormone resistance--a case report.

Auteurs : Ines Velez [États-Unis] ; Melanie Bond ; Steven Ellen ; Diane Ede-Nichols ; Jose Larumbe ; Victor Oramas ; Daniel Arnold

Source :

The Journal of clinical pediatric dentistry [ 1053-4628 ] ; 2009.

RBID : pubmed:19953813

Descripteurs français

English descriptors

KwdEn :
- Adolescent (MeSH), Bone Diseases, Metabolic (diagnostic imaging), Bone Diseases, Metabolic (etiology), Dental Enamel Hypoplasia (diagnostic imaging), Dental Enamel Hypoplasia (etiology), Dentigerous Cyst (diagnostic imaging), Dentigerous Cyst (etiology), Female (MeSH), Humans (MeSH), Jaw Diseases (diagnostic imaging), Jaw Diseases (etiology), Parathyroid Hormone (metabolism), Pseudohypoparathyroidism (complications), Pseudohypoparathyroidism (metabolism), Radiography (MeSH), Tooth, Impacted (diagnostic imaging), Tooth, Impacted (etiology), Vitamin D (metabolism).
MESH :
- chemical , metabolism : Parathyroid Hormone, Vitamin D.
- complications : Pseudohypoparathyroidism.
- diagnostic imaging : Bone Diseases, Metabolic, Dental Enamel Hypoplasia, Dentigerous Cyst, Jaw Diseases, Tooth, Impacted.
- etiology : Bone Diseases, Metabolic, Dental Enamel Hypoplasia, Dentigerous Cyst, Jaw Diseases, Tooth, Impacted.
- metabolism : Pseudohypoparathyroidism.
- Adolescent, Female, Humans, Radiography.

Abstract

Hereditary Osteodystrophy, also called pseudohypoparathyroidism, Type 1A (PHP), is a very rare condition composed of a heterogeneous group of autosomal dominant disorders with the common feature of organ resistance to multiple hormones. These patients produce the right amount of hormones but there is resistance to its effect. PHP is difficult to diagnose and the lack of diagnosis may have serious implications for the patient. We report a case of PHP, diagnosed by the dentist, due to the dental and jaw manifestations.

DOI: 10.17796/jcpd.34.1.33017umx4n144285
PubMed: 19953813

Affiliations:

États-Unis

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Le document en format XML

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<author><name sortKey="Velez, Ines" sort="Velez, Ines" uniqKey="Velez I" first="Ines" last="Velez">Ines Velez</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent (MeSH)</term>
<term>Bone Diseases, Metabolic (diagnostic imaging)</term>
<term>Bone Diseases, Metabolic (etiology)</term>
<term>Dental Enamel Hypoplasia (diagnostic imaging)</term>
<term>Dental Enamel Hypoplasia (etiology)</term>
<term>Dentigerous Cyst (diagnostic imaging)</term>
<term>Dentigerous Cyst (etiology)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Jaw Diseases (diagnostic imaging)</term>
<term>Jaw Diseases (etiology)</term>
<term>Parathyroid Hormone (metabolism)</term>
<term>Pseudohypoparathyroidism (complications)</term>
<term>Pseudohypoparathyroidism (metabolism)</term>
<term>Radiography (MeSH)</term>
<term>Tooth, Impacted (diagnostic imaging)</term>
<term>Tooth, Impacted (etiology)</term>
<term>Vitamin D (metabolism)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent (MeSH)</term>
<term>Dent enclavée (imagerie diagnostique)</term>
<term>Dent enclavée (étiologie)</term>
<term>Femelle (MeSH)</term>
<term>Hormone parathyroïdienne (métabolisme)</term>
<term>Humains (MeSH)</term>
<term>Hypoplasie de l'émail dentaire (imagerie diagnostique)</term>
<term>Hypoplasie de l'émail dentaire (étiologie)</term>
<term>Kyste dentigère (imagerie diagnostique)</term>
<term>Kyste dentigère (étiologie)</term>
<term>Maladies de la mâchoire (imagerie diagnostique)</term>
<term>Maladies de la mâchoire (étiologie)</term>
<term>Maladies osseuses métaboliques (imagerie diagnostique)</term>
<term>Maladies osseuses métaboliques (étiologie)</term>
<term>Pseudohypoparathyroïdie (complications)</term>
<term>Pseudohypoparathyroïdie (métabolisme)</term>
<term>Radiographie (MeSH)</term>
<term>Vitamine D (métabolisme)</term>
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<term>Vitamin D</term>
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</keywords>
<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Bone Diseases, Metabolic</term>
<term>Dental Enamel Hypoplasia</term>
<term>Dentigerous Cyst</term>
<term>Jaw Diseases</term>
<term>Tooth, Impacted</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Bone Diseases, Metabolic</term>
<term>Dental Enamel Hypoplasia</term>
<term>Dentigerous Cyst</term>
<term>Jaw Diseases</term>
<term>Tooth, Impacted</term>
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<keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Dent enclavée</term>
<term>Hypoplasie de l'émail dentaire</term>
<term>Kyste dentigère</term>
<term>Maladies de la mâchoire</term>
<term>Maladies osseuses métaboliques</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Pseudohypoparathyroidism</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Hormone parathyroïdienne</term>
<term>Pseudohypoparathyroïdie</term>
<term>Vitamine D</term>
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<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Dent enclavée</term>
<term>Hypoplasie de l'émail dentaire</term>
<term>Kyste dentigère</term>
<term>Maladies de la mâchoire</term>
<term>Maladies osseuses métaboliques</term>
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<term>Female</term>
<term>Humans</term>
<term>Radiography</term>
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<front><div type="abstract" xml:lang="en">Hereditary Osteodystrophy, also called pseudohypoparathyroidism, Type 1A (PHP), is a very rare condition composed of a heterogeneous group of autosomal dominant disorders with the common feature of organ resistance to multiple hormones. These patients produce the right amount of hormones but there is resistance to its effect. PHP is difficult to diagnose and the lack of diagnosis may have serious implications for the patient. We report a case of PHP, diagnosed by the dentist, due to the dental and jaw manifestations.</div>
</front>
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<DateCompleted><Year>2010</Year>
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<DateRevised><Year>2019</Year>
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<Title>The Journal of clinical pediatric dentistry</Title>
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<ArticleTitle>Hereditary osteodystrophy with multiple hormone resistance--a case report.</ArticleTitle>
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<Abstract><AbstractText>Hereditary Osteodystrophy, also called pseudohypoparathyroidism, Type 1A (PHP), is a very rare condition composed of a heterogeneous group of autosomal dominant disorders with the common feature of organ resistance to multiple hormones. These patients produce the right amount of hormones but there is resistance to its effect. PHP is difficult to diagnose and the lack of diagnosis may have serious implications for the patient. We report a case of PHP, diagnosed by the dentist, due to the dental and jaw manifestations.</AbstractText>
</Abstract>
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<AffiliationInfo><Affiliation>Oral and Maxillofacial Pathology, Nova Southeastern University, College of Dental Medicine, USA. ivelez@nova.edu</Affiliation>
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<MeshHeading><DescriptorName UI="D011547" MajorTopicYN="N">Pseudohypoparathyroidism</DescriptorName>
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<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
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<name sortKey="Ede Nichols, Diane" sort="Ede Nichols, Diane" uniqKey="Ede Nichols D" first="Diane" last="Ede-Nichols">Diane Ede-Nichols</name>
<name sortKey="Ellen, Steven" sort="Ellen, Steven" uniqKey="Ellen S" first="Steven" last="Ellen">Steven Ellen</name>
<name sortKey="Larumbe, Jose" sort="Larumbe, Jose" uniqKey="Larumbe J" first="Jose" last="Larumbe">Jose Larumbe</name>
<name sortKey="Oramas, Victor" sort="Oramas, Victor" uniqKey="Oramas V" first="Victor" last="Oramas">Victor Oramas</name>
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<country name="États-Unis"><noRegion><name sortKey="Velez, Ines" sort="Velez, Ines" uniqKey="Velez I" first="Ines" last="Velez">Ines Velez</name>
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	Serveur d'exploration sur le suicide chez les dentistes
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Hereditary osteodystrophy with multiple hormone resistance--a case report.

Hereditary osteodystrophy with multiple hormone resistance--a case report.

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki