The Experts below are selected from a list of 321 Experts worldwide ranked by ideXlab platform
Christine Neumann - One of the best experts on this subject based on the ideXlab platform.
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A new family with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.
Journal of the American Academy of Dermatology, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Holger Hanssle, Christian Hallermann, Lutz Kretschmer, Christine NeumannAbstract:We describe a new family with the rare Genodermatosis keratosis punctata palmo-plantaris Buschke-Fischer-Brauer (keratoma disseminatum). In all, 3 family members in 3 generations were affected, a pattern consistent with autosomal dominant inheritance. Clinical symptoms started in the third decade with disseminated, small, round, hyperkeratotic papules on the palms and soles. Punctate keratoses coalesced into hyperkeratotic plaques on pressure points. Identification of additional families is necessary to permit definitive genetic classification of this Genodermatosis.
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47 patients in 14 families with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer
European journal of dermatology : EJD, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Lutz Kretschmer, Hans Christian Hennies, Holger A. Haenssle, Christine NeumannAbstract:We summarize the clinical data of 47 patients with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer. The pedigrees of 14 German families were studied. In three families there was only one member affected, two or more affected members were found in the other families. These family pedigrees were consistent with autosomal dominant inheritance. Variable expression of the disease was noted in members within one family. Over pressure points punctate keratoses coalesced into hyperkeratotic plaques. There was palmoplantar hyperhidrosis in 3 families associated with keratosis. Continuous systemic retinoid treatment can clear symptoms. Future genetic classification on a molecular basis may reveal the existance of more than one entity of this clinically heterogeneous Genodermatosis.
Steffen Emmert - One of the best experts on this subject based on the ideXlab platform.
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A new family with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.
Journal of the American Academy of Dermatology, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Holger Hanssle, Christian Hallermann, Lutz Kretschmer, Christine NeumannAbstract:We describe a new family with the rare Genodermatosis keratosis punctata palmo-plantaris Buschke-Fischer-Brauer (keratoma disseminatum). In all, 3 family members in 3 generations were affected, a pattern consistent with autosomal dominant inheritance. Clinical symptoms started in the third decade with disseminated, small, round, hyperkeratotic papules on the palms and soles. Punctate keratoses coalesced into hyperkeratotic plaques on pressure points. Identification of additional families is necessary to permit definitive genetic classification of this Genodermatosis.
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47 patients in 14 families with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer
European journal of dermatology : EJD, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Lutz Kretschmer, Hans Christian Hennies, Holger A. Haenssle, Christine NeumannAbstract:We summarize the clinical data of 47 patients with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer. The pedigrees of 14 German families were studied. In three families there was only one member affected, two or more affected members were found in the other families. These family pedigrees were consistent with autosomal dominant inheritance. Variable expression of the disease was noted in members within one family. Over pressure points punctate keratoses coalesced into hyperkeratotic plaques. There was palmoplantar hyperhidrosis in 3 families associated with keratosis. Continuous systemic retinoid treatment can clear symptoms. Future genetic classification on a molecular basis may reveal the existance of more than one entity of this clinically heterogeneous Genodermatosis.
Markus Zutt - One of the best experts on this subject based on the ideXlab platform.
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A new family with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.
Journal of the American Academy of Dermatology, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Holger Hanssle, Christian Hallermann, Lutz Kretschmer, Christine NeumannAbstract:We describe a new family with the rare Genodermatosis keratosis punctata palmo-plantaris Buschke-Fischer-Brauer (keratoma disseminatum). In all, 3 family members in 3 generations were affected, a pattern consistent with autosomal dominant inheritance. Clinical symptoms started in the third decade with disseminated, small, round, hyperkeratotic papules on the palms and soles. Punctate keratoses coalesced into hyperkeratotic plaques on pressure points. Identification of additional families is necessary to permit definitive genetic classification of this Genodermatosis.
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47 patients in 14 families with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer
European journal of dermatology : EJD, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Lutz Kretschmer, Hans Christian Hennies, Holger A. Haenssle, Christine NeumannAbstract:We summarize the clinical data of 47 patients with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer. The pedigrees of 14 German families were studied. In three families there was only one member affected, two or more affected members were found in the other families. These family pedigrees were consistent with autosomal dominant inheritance. Variable expression of the disease was noted in members within one family. Over pressure points punctate keratoses coalesced into hyperkeratotic plaques. There was palmoplantar hyperhidrosis in 3 families associated with keratosis. Continuous systemic retinoid treatment can clear symptoms. Future genetic classification on a molecular basis may reveal the existance of more than one entity of this clinically heterogeneous Genodermatosis.
Lutz Kretschmer - One of the best experts on this subject based on the ideXlab platform.
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A new family with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.
Journal of the American Academy of Dermatology, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Holger Hanssle, Christian Hallermann, Lutz Kretschmer, Christine NeumannAbstract:We describe a new family with the rare Genodermatosis keratosis punctata palmo-plantaris Buschke-Fischer-Brauer (keratoma disseminatum). In all, 3 family members in 3 generations were affected, a pattern consistent with autosomal dominant inheritance. Clinical symptoms started in the third decade with disseminated, small, round, hyperkeratotic papules on the palms and soles. Punctate keratoses coalesced into hyperkeratotic plaques on pressure points. Identification of additional families is necessary to permit definitive genetic classification of this Genodermatosis.
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47 patients in 14 families with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer
European journal of dermatology : EJD, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Lutz Kretschmer, Hans Christian Hennies, Holger A. Haenssle, Christine NeumannAbstract:We summarize the clinical data of 47 patients with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer. The pedigrees of 14 German families were studied. In three families there was only one member affected, two or more affected members were found in the other families. These family pedigrees were consistent with autosomal dominant inheritance. Variable expression of the disease was noted in members within one family. Over pressure points punctate keratoses coalesced into hyperkeratotic plaques. There was palmoplantar hyperhidrosis in 3 families associated with keratosis. Continuous systemic retinoid treatment can clear symptoms. Future genetic classification on a molecular basis may reveal the existance of more than one entity of this clinically heterogeneous Genodermatosis.
Wolfgang Küster - One of the best experts on this subject based on the ideXlab platform.
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A new family with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.
Journal of the American Academy of Dermatology, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Holger Hanssle, Christian Hallermann, Lutz Kretschmer, Christine NeumannAbstract:We describe a new family with the rare Genodermatosis keratosis punctata palmo-plantaris Buschke-Fischer-Brauer (keratoma disseminatum). In all, 3 family members in 3 generations were affected, a pattern consistent with autosomal dominant inheritance. Clinical symptoms started in the third decade with disseminated, small, round, hyperkeratotic papules on the palms and soles. Punctate keratoses coalesced into hyperkeratotic plaques on pressure points. Identification of additional families is necessary to permit definitive genetic classification of this Genodermatosis.
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47 patients in 14 families with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer
European journal of dermatology : EJD, 2003Co-Authors: Steffen Emmert, Wolfgang Küster, Markus Zutt, Lutz Kretschmer, Hans Christian Hennies, Holger A. Haenssle, Christine NeumannAbstract:We summarize the clinical data of 47 patients with the rare Genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer. The pedigrees of 14 German families were studied. In three families there was only one member affected, two or more affected members were found in the other families. These family pedigrees were consistent with autosomal dominant inheritance. Variable expression of the disease was noted in members within one family. Over pressure points punctate keratoses coalesced into hyperkeratotic plaques. There was palmoplantar hyperhidrosis in 3 families associated with keratosis. Continuous systemic retinoid treatment can clear symptoms. Future genetic classification on a molecular basis may reveal the existance of more than one entity of this clinically heterogeneous Genodermatosis.