X-linked intellectual disability, Stoll type

MONDO:0019423

X-linked intellectual disability, Stoll type is characterized by intellectual deficit, short stature and characteristic facies (hypertelorism, prominent forehead, frontal bossing, a broad nasal tip and anteverted nares). It has been described in four males from three generations of the same family. Two females from this family also displayed intellectual deficit and the characteristic facies. Transmission is X-linked.

0 clinical trials for this condition and its sub-types, 0 tagged with X-linked intellectual disability, Stoll type itself.

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↑ Congenital nervous system disorder (284) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ X-linked syndromic intellectual disability (12)

Including sub-types (0) Tagged with X-linked intellectual disability, Stoll type (0)

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