Myhre syndrome is a rare disorder characterized by low birthweight, short stature, mental
retardation, facial dysmorphism (blepharophimosis, midfacial hypoplasia, prognathism) …

Myhre Syndrome is a rare condition associated with mental retardation, short stature,
generalized muscle hypertrophy, cardiac defects and a distinct facial appearance. There …

Myhre syndrome is a clinically distinct syndrome with multiple system involvement. It was
first described in 1981 by Myhre et al.(1981) in two unrelated patients. The condition was …

We report the fifth female patient with Myhre syndrome (MS) and review the literature. She is
a 13-year-old Mexican girl whose phenotype fulfills all the clinical and radiological criteria …

Myhre's syndrome is a rare genetic condition first described in 1981 by Myhre et al.[1981].
Additional cases of Myhre's syndrome were reported [Soljiak et al., 1983; Garcia-Cruz et al …

Garcia‐Cruz D, Figuera LE, Feria‐Velazco A, Sanchez‐Corona J, Garcia‐Cruz MO, Ramirez‐
Dueñas RM, Hernandez‐Cordova A, Ruiz MX, Bitar‐Alatorre WE, Ramirez‐Dueñas ML …

Abstract Myhre syndrome (MS)(MIM 139210) is a rare disorder characterized by short
stature, mental retardation, muscular build, blepharophimosis, and decreased joint mobility …

We describe the clinical characteristics of 4 singleton cases, 3 males and 1 female, with
Myhre Syndrome (OMIM 139210), who were born to non-consanguineous parents. Three …

Myhre syndrome (MIM 139210) is a rare disorder, which was first described 30 years ago in
two unrelated boys with mental retardation, short stature, muscular hypertrophy, and limited …

Aims: Myhre syndrome is a rare disorder characterized by abnormal growth of the skeleton,
muscles, and joints. The relationship of this syndrome to craniofacial growth and …