Objective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak syndrome, as a result of bleeding diathesis. Clinical Presentation and Intervention. A 23-year-old male presented with recurrent epistaxis and, upon physical examination, was found to be remarkable for albinism and suborbital ecchymosis. The absence of dense bodies in the platelets was demonstrated using electron microscopy. This patient was (slowly) administered one unit of a platelet suspension, and his bleeding decreased considerably. Conclusion. This case shows that Hermansky-Pudlak syndrome should be considered in the differential diagnosis of a patient presenting with bleeding diathesis, when the clinical presentation also includes ocu...
Griscelli syndrome (GS) was diagnosed in a 2-year-old patient with oculocutaneous albinism and immun...
Abstract Background Hermansky-Pudlak syndrome (HPS) is a rare, genetically heterogeneous disorder th...
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive genetic disorder in which the proper funct...
Hermansky-Pudlak syndrome is a rare autosomal recessive multisystem disease, with oculocutneous albi...
Hermansky-Pudlak syndrome (HPS) is a rare form of syndromic oculocutaneous albinism caused by disord...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which results in oculocutane...
Abstract Background Determining the etiology of oculocutaneous albinism is important for proper clin...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder caused by defects in 10 human...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the...
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder, the most common complication of which in...
The albinotic skin and hair of 2 patients with Hermansky-Pudlak syndrome were investigated by light ...
Hermansky-Pudlak syndrome (HPS) associates oculocutaneous albinism and systemic affections including...
Hermansky-Pudlak syndrome is a rare syndrome characterized by bleeding diathesis due to platelet dys...
Hermansky-Pudlak syndrome (HPS) is a heterogeneous disorder combining oculocutaneous albinism (OCA) ...
PubMedID: 24284295Hermansky-Pudlak Syndrome (HPS) is a rare autosomal recessive disorder presenting ...
Griscelli syndrome (GS) was diagnosed in a 2-year-old patient with oculocutaneous albinism and immun...
Abstract Background Hermansky-Pudlak syndrome (HPS) is a rare, genetically heterogeneous disorder th...
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive genetic disorder in which the proper funct...
Hermansky-Pudlak syndrome is a rare autosomal recessive multisystem disease, with oculocutneous albi...
Hermansky-Pudlak syndrome (HPS) is a rare form of syndromic oculocutaneous albinism caused by disord...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which results in oculocutane...
Abstract Background Determining the etiology of oculocutaneous albinism is important for proper clin...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder caused by defects in 10 human...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the...
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder, the most common complication of which in...
The albinotic skin and hair of 2 patients with Hermansky-Pudlak syndrome were investigated by light ...
Hermansky-Pudlak syndrome (HPS) associates oculocutaneous albinism and systemic affections including...
Hermansky-Pudlak syndrome is a rare syndrome characterized by bleeding diathesis due to platelet dys...
Hermansky-Pudlak syndrome (HPS) is a heterogeneous disorder combining oculocutaneous albinism (OCA) ...
PubMedID: 24284295Hermansky-Pudlak Syndrome (HPS) is a rare autosomal recessive disorder presenting ...
Griscelli syndrome (GS) was diagnosed in a 2-year-old patient with oculocutaneous albinism and immun...
Abstract Background Hermansky-Pudlak syndrome (HPS) is a rare, genetically heterogeneous disorder th...
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive genetic disorder in which the proper funct...