syndrome with late onset axonal neuropathy McLeod syndrome is a rare multisystem disorder defined by weak expression of the Kell glycoprotein antigens and the absence of a red blood cell surface antigen, Kx.1 2 The gene responsible for McLeod syndrome, XK, was cloned in 1994.1 The XK protein contains the Kx antigen missing in patients with McLeod syndrome. Mutation analysis of the XK gene has shown different deletions or point mutations in families with this condition.2 3 Clinical features of McLeod syndrome are reported to be heterogeneous.2 4 5 Clinica
CLINICAL CHARACTERISTICS: McLeod neuroacanthocytosis syndrome (designated as MLS throughout this rev...
BACKGROUND: McLeod syndrome (MLS) is hematologically defined by the absence of the red blood cell (R...
McLeod syndrome (MLS) is a very rare genetic X-linked condition due to XK gene mutations and charact...
McLeod syndrome is caused by mutations of XK, an X-chromosomal gene of unknown function. Originally ...
BACKGROUND: The X-linked McLeod neuroacanthocytosis syndrome is a multisystem disorder with hematolo...
McLeod syndrome is an X-linked multisystem disorder characterized by abnormalities in the neuromuscu...
The X-linked McLeod syndrome is defined by absent Kx red blood cell antigen and weak expression of K...
The McLeod syndrome is an X-linked disorder caused by mutations of the XK gene encoding the XK prote...
McLeod syndrome (MLS) is a rare adult-onset, progressive and incurable X-linked multisystemic disord...
Importance McLeod syndrome, encoded by the gene XK, is a rare and progressive disease that shares im...
Multisystem deterioration occurs mainly in older individuals and may be related to physiological tis...
McLeod syndrome is an X-linked recessive disorder, characterized by neuromuscular and hematopoietic ...
AbstractWe present a 70-year-old male patient of Greek origin with choreatic movements of the tongue...
We report a family with three members affected by a typically X-linked McLeod syndrome. In the proba...
McLeod syndrome, characterized by acanthocytosis and the absence of a red-blood-cell Kell antigen (K...
CLINICAL CHARACTERISTICS: McLeod neuroacanthocytosis syndrome (designated as MLS throughout this rev...
BACKGROUND: McLeod syndrome (MLS) is hematologically defined by the absence of the red blood cell (R...
McLeod syndrome (MLS) is a very rare genetic X-linked condition due to XK gene mutations and charact...
McLeod syndrome is caused by mutations of XK, an X-chromosomal gene of unknown function. Originally ...
BACKGROUND: The X-linked McLeod neuroacanthocytosis syndrome is a multisystem disorder with hematolo...
McLeod syndrome is an X-linked multisystem disorder characterized by abnormalities in the neuromuscu...
The X-linked McLeod syndrome is defined by absent Kx red blood cell antigen and weak expression of K...
The McLeod syndrome is an X-linked disorder caused by mutations of the XK gene encoding the XK prote...
McLeod syndrome (MLS) is a rare adult-onset, progressive and incurable X-linked multisystemic disord...
Importance McLeod syndrome, encoded by the gene XK, is a rare and progressive disease that shares im...
Multisystem deterioration occurs mainly in older individuals and may be related to physiological tis...
McLeod syndrome is an X-linked recessive disorder, characterized by neuromuscular and hematopoietic ...
AbstractWe present a 70-year-old male patient of Greek origin with choreatic movements of the tongue...
We report a family with three members affected by a typically X-linked McLeod syndrome. In the proba...
McLeod syndrome, characterized by acanthocytosis and the absence of a red-blood-cell Kell antigen (K...
CLINICAL CHARACTERISTICS: McLeod neuroacanthocytosis syndrome (designated as MLS throughout this rev...
BACKGROUND: McLeod syndrome (MLS) is hematologically defined by the absence of the red blood cell (R...
McLeod syndrome (MLS) is a very rare genetic X-linked condition due to XK gene mutations and charact...