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Microcephaly with or without short stature
MONDO:0100346Primary microcephaly refers to the clinical finding of a head circumference more than than 3 standard deviations (SD) below the age- and sex-related mean, present at birth. Primary microcephaly is a static developmental anomaly, distinguished from secondary microcephaly, which refers to a progressive neurodegenerative condition. Microcephaly is a disorder of fetal brain growth; individuals with microcephaly have small brains and almost always have intellectual disability, although rare individuals with mild microcephaly (-3 SD) and normal intelligence have been reported. Additional clinical features may include short stature or mild seizures. These clinical features include Seckel syndrome, a rare autosomal recessive disorder characterized by intrauterine growth retardation, dwarfism, microcephaly with intellectual disability.
8 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly with or without short stature itself.
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Browse by category →Sub-types of Microcephaly with or without short stature
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Microcephaly 6 with or without short stature 0 trials · 8 incl. sub-types
2 sub-types
- Microcephaly 6, primary, autosomal recessive 8 trials
- Seckel syndrome 4 0 trials