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Fig. 3 | BMC Medical Genetics

Fig. 3

From: Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy

Fig. 3

Pedigree and audiological phenotype of Family 3. a Pedigree of Family 3. The affected subject is coloured black, the proband is indicated by an arrow, unaffected members with black spots indicate obligate carriers of the causative variation, and a rhombus with a question mark is a subject with unknown gender. b Audiograms of the proband (III:5) and his mother (II:5). c Speech recognition score (SRS) of the proband upon different stimulations, showing different tendency from normal controls. d Normal DPOAE result of the proband. e Absence of ABR waves and present CM waves in the proband. f Electrocochleography (ECochG) showed abnormal -SP/AP > 0.4. L, left, blue; R, right, red

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