Add to ORKGThe presence of giant organelles in the cytoplasm of peripheral blood elements is diagnostic for the Chediak-Higashi syndrome. These abnormal cytoplasmic inclusions are found within neutrophils, eosinophils, basophils, lymphocytes, monocytes, and platelets. Their fine structural characteristics differ. Neutrophils demonstrate striking variability in the size, shape, and internal features of their giant organelles. Lymphocytes contain two different types of giant inclusions, one with a smoothly homogeneous substructure, the other with structures resembling microtubules. Emphasizing the ultrastructural similarities and differences of these anomalous granulations may provide valuable clues for understanding the basic defect of this inherited d...
Review on Chediak-Higashi Syndrome, with data on clinics, and the genes involved
AbstractChediak–Higashi syndrome (CHS) is a rare autosomal recessive lysosomal disorder characterize...
Background. Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive disorder characterized by ...
Chediak higashi Syndrome (CHS) is a rare autosomal recessive multisystem disorder with a defect in g...
Chediak Higashi syndrome (CHS) is a rare autosomal recessive immunodeficiency disorder that arises d...
Introduction: Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disorder characterized by...
Chediak-Higashi Syndrome is a pathology caused by a mutation in the LYST gene, characterized by immu...
Endemic Chediak-Higashi Syndrome occurs in a restricted geographic area (Pregonero, State of T#{225}...
Chediak Higashi Syndrome is a rare inherited autosomal recessive disorder of immune system. Suscepti...
Blood leukocytes from a patient with Chediak-Higashi syndrome (CHS) were compared with normal cells ...
Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive disorder characterized by hypopigmenta...
genetic disorder of children and certain animal species including the beige mouse. We have previousl...
Chediak-Higashi syndrome (CHS) is a very rare autosomal recessive immunodefiency disorder char-acter...
The Chediak-Higashi syndrome (CHS) is a rare form of partial albinism which was initially recog-nize...
Hermansky-Pudlak syndrome (HPS) is a disorder of lysosome-related organelle biogenesis that displays...
Review on Chediak-Higashi Syndrome, with data on clinics, and the genes involved
AbstractChediak–Higashi syndrome (CHS) is a rare autosomal recessive lysosomal disorder characterize...
Background. Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive disorder characterized by ...
Chediak higashi Syndrome (CHS) is a rare autosomal recessive multisystem disorder with a defect in g...
Chediak Higashi syndrome (CHS) is a rare autosomal recessive immunodeficiency disorder that arises d...
Introduction: Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disorder characterized by...
Chediak-Higashi Syndrome is a pathology caused by a mutation in the LYST gene, characterized by immu...
Endemic Chediak-Higashi Syndrome occurs in a restricted geographic area (Pregonero, State of T#{225}...
Chediak Higashi Syndrome is a rare inherited autosomal recessive disorder of immune system. Suscepti...
Blood leukocytes from a patient with Chediak-Higashi syndrome (CHS) were compared with normal cells ...
Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive disorder characterized by hypopigmenta...
genetic disorder of children and certain animal species including the beige mouse. We have previousl...
Chediak-Higashi syndrome (CHS) is a very rare autosomal recessive immunodefiency disorder char-acter...
The Chediak-Higashi syndrome (CHS) is a rare form of partial albinism which was initially recog-nize...
Hermansky-Pudlak syndrome (HPS) is a disorder of lysosome-related organelle biogenesis that displays...
Review on Chediak-Higashi Syndrome, with data on clinics, and the genes involved
AbstractChediak–Higashi syndrome (CHS) is a rare autosomal recessive lysosomal disorder characterize...
Background. Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive disorder characterized by ...