Radioulnar synostosis with amegakaryocytic thrombocytopenia 1- MedGen UID:
- 1637913
- •Concept ID:
- C4551975
- •
- Disease or Syndrome
Radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT) is characterized by thrombocytopenia that progresses to pancytopenia, in association with congenital proximal fusion of the radius and ulna that results in extremely limited pronation and supination of the forearm (summary by Niihori et al., 2015).
Genetic Heterogeneity of Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia
Radioulnar synostosis with amegakaryocytic thrombocytopenia-2 (RUSAT2; 616738) is caused by heterozygous mutation in the MECOM gene (165215) on chromosome 3q26.
Immunodeficiency 91 and hyperinflammation- MedGen UID:
- 1794283
- •Concept ID:
- C5562073
- •
- Disease or Syndrome
Immunodeficiency-91 and hyperinflammation (IMD91) is an autosomal recessive complex immunologic disorder characterized by both immunodeficiency and recurrent infections, often to viruses or mycobacteria, as well as by hyperinflammation with systemic involvement. Affected individuals present in infancy with variable features, including fever, infection, thrombocytopenia, renal or hepatic dysfunction, recurrent infections, or seizures. Most patients eventually develop hepatic or renal failure, compromised neurologic function, lymphadenopathy or hepatosplenomegaly, and multiorgan failure resulting in death. More variable features may include intermittent monocytosis, features of hemophagocytic lymphohistiocytosis (HLH), and serologic evidence of hyperinflammation. The disorder is thought to result from dysregulation of the interferon response to viral stimulation in the innate immune system (summary by Le Voyer et al., 2021; Vavassori et al., 2021).
Braddock-carey syndrome 2- MedGen UID:
- 1823962
- •Concept ID:
- C5774189
- •
- Disease or Syndrome
Braddock-Carey syndrome-2 (BRDCS2) is characterized by congenital thrombocytopenia, microcephaly, and facial dysmorphisms including Pierre-Robin sequence (Sleiman et al., 2017).
For a general phenotypic description and discussion of genetic heterogeneity of Braddock-Carey syndrom, see BRCDS1 (619980).
Congenital amegakaryocytic thrombocytopenia 1- MedGen UID:
- 1052544
- •Concept ID:
- CN377202
- •
- Disease or Syndrome
Congenital amegakaryocytic thrombocytopenia-1 (CAMT1) is an autosomal recessive disorder characterized by onset of thrombocytopenia and megakaryocytopenia in infancy or early childhood. The disorder is progressive and evolves to pancytopenia and bone marrow failure. Serum thrombopoietin is elevated. There is a favorable response to bone marrow transplantation (Muraoka et al., 1997; King et al., 2005).
Genetic Heterogeneity of Congenital Amegakaryocytic Thrombocytopenia
CAMT2 (620481) is caused by mutation in the THPO gene (600044) on chromosome 3q27.