Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells

Also Known As:

Networked: 9 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1.	Thrombasthenia (Glanzmann Thrombasthenia)
2.	Hermanski-Pudlak Syndrome (Hermansky-Pudlak Syndrome)
3.	Hemorrhage
4.	Cerebral Hemorrhage
5.	Bernard-Soulier Syndrome (Giant Platelet Syndrome)

Experts

1.	Alberelli, Maria Adele: 1 article (12/2019)
2.	Bacci, Monica: 1 article (12/2019)
3.	De Candia, Erica: 1 article (12/2019)
4.	Dragani, Alfredo: 1 article (12/2019)
5.	Falanga, Anna: 1 article (12/2019)
6.	Ferrazzi, Paola: 1 article (12/2019)
7.	Gamba, Sara: 1 article (12/2019)
8.	Landolfi, Raffaele: 1 article (12/2019)
9.	Lodigiani, Corrado: 1 article (12/2019)
10.	Marchetti, Marina: 1 article (12/2019)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells:

1.	Serotonin (5 Hydroxytryptamine)IBA 07/01/2001 - "Delta-storage pool disease in infancy with absence of blood serotonin associated with psychomotor retardation." 01/01/2019 - "Spontaneous Intracerebral Hemorrhage Due to Delta Storage Pool Disease in a Patient on a Serotonin-Norepinephrine Reuptake Inhibitor." 01/01/2019 - "We report a case of spontaneous intracerebral hemorrhage (sICH) due to delta storage pool disease in a 60-year-old female on a serotonin-norepinephrine reuptake inhibitor (SNRI). " 01/01/1992 - "This thrombopathy is a pure delta storage pool disease (SPD), as evidenced: a) biochemically by platelet serotonin content and metabolism and by comparative ATP/ADP content and secretion; b) functionally by reduced aggregability to low concentrations of convulxin and collagen but normal aggregability to other agents and normal synthesis of thromboxane B2. "
2.	Adenosine Diphosphate (ADP)IBA 09/01/1995 - "Inherited platelet delta-storage pool disease in dogs causing severe bleeding: an animal model for a specific ADP deficiency." 01/01/1992 - "This thrombopathy is a pure delta storage pool disease (SPD), as evidenced: a) biochemically by platelet serotonin content and metabolism and by comparative ATP/ADP content and secretion; b) functionally by reduced aggregability to low concentrations of convulxin and collagen but normal aggregability to other agents and normal synthesis of thromboxane B2. "
3.	Prostaglandin H2 Thromboxane A2 ReceptorsIBA 08/01/2015 - "Severe bleeds requiring blood transfusions were observed in 50% of deliveries in Glanzmann thrombasthenia (GT), but not in the patients with delta storage pool disease, Hermansky-Pudlak syndrome, P2Y12 defect or defect of thromboxane A2 receptor. "
4.	GTP-Binding Proteins (G-Protein)IBA 12/01/2007 - "Classical thrombopathies involve disorders of platelet adhesion such as Glanzmann thrombastenia and Bernard-Soulier syndrome, defective G protein signalling diseases with impaired phospholipase C activation, and abnormal platelet granule secretion disorders such as gray platelet disorder and delta-storage pool disease. "
5.	Vasopressins (Vasopressin)IBA 07/01/1999 - "[Thrombocytic alpha-delta-storage-pool-disease: shortening of bleeding time after infusion of 1-desamino-8-D-arginine vasopressin]."
6.	Thromboxane B2IBA 01/01/1992 - "This thrombopathy is a pure delta storage pool disease (SPD), as evidenced: a) biochemically by platelet serotonin content and metabolism and by comparative ATP/ADP content and secretion; b) functionally by reduced aggregability to low concentrations of convulxin and collagen but normal aggregability to other agents and normal synthesis of thromboxane B2. "
7.	PolyphosphatesIBA 02/01/2009 - "Platelet inorganic polyphosphate decreases in patients with delta storage pool disease."
8.	Type C PhospholipasesIBA 12/01/2007 - "Classical thrombopathies involve disorders of platelet adhesion such as Glanzmann thrombastenia and Bernard-Soulier syndrome, defective G protein signalling diseases with impaired phospholipase C activation, and abnormal platelet granule secretion disorders such as gray platelet disorder and delta-storage pool disease. "
9.	Norepinephrine (Noradrenaline)FDA LinkGeneric 01/01/2019 - "Spontaneous Intracerebral Hemorrhage Due to Delta Storage Pool Disease in a Patient on a Serotonin-Norepinephrine Reuptake Inhibitor." 01/01/2019 - "We report a case of spontaneous intracerebral hemorrhage (sICH) due to delta storage pool disease in a 60-year-old female on a serotonin-norepinephrine reuptake inhibitor (SNRI). "
10.	CollagenIBA 01/01/1992 - "This thrombopathy is a pure delta storage pool disease (SPD), as evidenced: a) biochemically by platelet serotonin content and metabolism and by comparative ATP/ADP content and secretion; b) functionally by reduced aggregability to low concentrations of convulxin and collagen but normal aggregability to other agents and normal synthesis of thromboxane B2. "

Therapies and Procedures

1.	Blood Transfusion (Blood Transfusions) 08/01/2015 - "Severe bleeds requiring blood transfusions were observed in 50% of deliveries in Glanzmann thrombasthenia (GT), but not in the patients with delta storage pool disease, Hermansky-Pudlak syndrome, P2Y12 defect or defect of thromboxane A2 receptor. "