Disease #01672 (EAOH (ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (EAOH)), OMIM:208920)

Official abbreviation EAOH
Name ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (EAOH)
OMIM ID 208920
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 59
Phenotype entries for this disease 59
Associated with 1 gene APTX
Associated tissues -
Disease features -
Remarks -


Individuals

59 entries on 1 page. Showing entries 1 - 59.
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00034767 - - - - - Germany - - 0 - - EAOH ataxia with oculomotor apraxia type 1 APTX APTX 1 1 Andreas Laner
00208922 - PubMed: Tranchant 2003 brother/sister - - - - - 0 - - EAOH gait ataxia, mild axial and limb ataxia, dysarthria, areflexia, loss of pallesthesia, cerebellar atrophy, decreased motor conduction in lower limbs, right extensor plantar response, mild upper limb dystonia, moderate ptosis of the left lid, pes cavus, APTX APTX 2 1 Sergio Piñeiro
00208923 - PubMed: Le Ber 2003 - - - - - - 0 - - EAOH cerebellar ataxia, oculomotor apraxia, severe choria, dystonia face + hand, dysexecurive syndrome, abolished tendon reflexes, severe motor deficit, severe distal amyotrophy, decreased superficial sensory, moderate decreased vibration sense, pes cavus, scoliosis APTX APTX 1 1 Sergio Piñeiro
00208924 - PubMed: Moreira 2001 2-generation family, unaffected parents - - Portugal Portuguese - 0 - - EAOH typical AOA1 phenotype + marked dystonia and masklike faces APTX APTX 3 1 Sergio Piñeiro
00208925 - PubMed: Shimazaki 2002 - - - Japan Japanese - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208926 - PubMed: Criscuolo 2004 - - - Italy Italian - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208927 - PubMed: Moreira 2001 - - - Japan Japanese - 0 - - EAOH ataxia, ophthalmoparesis, nystagmus, mild mental retardation APTX APTX 1 1 Sergio Piñeiro
00208928 - PubMed: Moreira 2001 - - - Japan Japanese - 0 - - EAOH cerebellar ataxia, ocular apraxia, ...(not complete clinical information). APTX APTX 1 1 Sergio Piñeiro
00208929 - PubMed: Criscuolo 2005 - - - - - - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208931 - PubMed: Moreira 2001 - - - Japan Japanese - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208932 - PubMed: Moreira 2001 - - - Japan Japanese - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208933 - PubMed: Moreira 2001 - - - Japan Japanese - 0 - - EAOH gait ataxia, ocular apaxia, hyporeflexia, dysarthria, cerebellar atrophy, severe mental retardation (before ataxia onset) APTX APTX 2 1 Sergio Piñeiro
00208934 - PubMed: Ferrarini 2007 - - - - - - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208935 - - - - - Japan Japanese - 0 - - EAOH - APTX APTX 2 1 Sergio Piñeiro
00208937 - PubMed: Mosesso 2005 - - - - - - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208938 - PubMed: H'mida-Ben Brahim 2011 - - - Lebanon - - 0 - - EAOH - APTX APTX 1 1 Sergio Piñeiro
00208939 - PubMed: Date 2001 - - - Japan Japanese - 0 - - EAOH progressive ataxia, absence of tendon reflexes, distal loss of sense of position and vibration, pyramidal weakness of the legs, hypoalbuminemia APTX APTX 2 1 Sergio Piñeiro
00208940 - PubMed: Le Ber 2003 - - - - - - 0 - - EAOH cerebellar ataxia, dysexecurive syndrome, abolished tendon reflexes, severe motor deficit, moderate distal amyotrophy, decreased superficial sensory, moderate decreased vibration sense, scoliosis APTX APTX 2 1 Sergio Piñeiro
00208941 - PubMed: Le Ber 2003 - - - - - - 0 - - EAOH cerebellar ataxia, choria, dystonia hand, dysexecurive syndrome, abolished tendon reflexes, severe motor deficit, moderate distal amyotrophy, decreased superficial sensory, moderate decreased vibration sense APTX APTX 2 1 Sergio Piñeiro
00208942 - PubMed: Le Ber 2003 - - - - - - 0 - - EAOH cerebellar ataxia, oculomotor apraxia, choria, dystonia face + hand, mental retardation, abolished tendon reflexes, severe motor deficit, severe distal amyotrophy, decreased superficial sensory, moderate decreased vibration sense, limb oedema APTX APTX 2 1 Sergio Piñeiro
00208943 - PubMed: Le Ber 2003 - - - - - - 0 - - EAOH cerebellar ataxia, oculomotor apraxia, choria, dystonia face + hand, mental retardation, abolished tendon reflexes, severe motor deficit, severe distal amyotrophy, decreased superficial sensory, moderate decreased vibration sense, limb oedemam pes cavus, scoliosis APTX APTX 2 1 Sergio Piñeiro
00208944 - PubMed: Moreira 2001 - - - Portugal Portuguese - 0 - - EAOH cerebellar ataxia, ocular apraxia, ...(not complete clinical information). APTX APTX 1 1 Sergio Piñeiro
00208945 - PubMed: Moreira 2001 - - - Portugal Portuguese - 0 - - EAOH cerebellar ataxia, ocular apraxia, ...(not complete clinical information). APTX APTX 1 1 Sergio Piñeiro
00208946 - PubMed: Moreira 2001 - - - Portugal Portuguese - 0 - - EAOH cerebellar ataxia, ocular apraxia, ...(not complete clinical information). APTX APTX 1 1 Sergio Piñeiro
00208947 - PubMed: Moreira 2001 - - - Portugal Portuguese - 0 - - EAOH cerebellar ataxia, ocular apraxia, ...(not complete clinical information). APTX APTX 1 1 Sergio Piñeiro
00208948 - PubMed: Moreira 2001 - - - Portugal Portuguese - 0 - - EAOH cerebellar ataxia, ocular apraxia, ...(not complete clinical information). APTX APTX 1 1 Sergio Piñeiro
00208949 - PubMed: Date 2001 - - - Japan Japanese - 0 - - EAOH progressive ataxia, absence of tendon reflexes, distal loss of sense of position and vibration, pyramidal weakness of the legs, hypoalbuminemia APTX APTX 2 1 Sergio Piñeiro
00208950 - PubMed: Crimella 2011 - - - - - - 0 - - EAOH ataxic gait, dysmetria, diffuse distal leg and hand hypotrophy, absence of deep tendon reflexes (DTR), pes , cavus, with intact strength and sensation, dysarthria, difficulties in visual pursuit with ocular , esotropia, flaccid tetraplegia, severe hypotrophy, hypotonia and areflexia. severe axonal neuropathy more severe at the lower limbs. Severe cerebellar atrophy. APTX APTX 1 1 Sergio Piñeiro
00208951 - PubMed: Castellotti 2011 - - - - - - 0 - - EAOH Severe gait limb ataxia. Moderate dysarthria, defects of saccadic initiation and choreoathetosis. Mild distal weakness lower and upper limbs, muscular wasting, cognitive impairment and decreased vibration sense lower limbs. Nystagmus, Babinksi sign and deep tendon reflexes lower limbs absent. APTX APTX 1 1 Sergio Piñeiro
00208952 - - - - - - - - 0 - - EAOH Moderate gait limb ataxia. Mild dysarthria. Metal retardation and deep tendon reflexes lower limbs absent. APTX APTX 2 1 Sergio Piñeiro
00208953 - PubMed: Castellotti 2011 - - - - - - 0 - - EAOH Severe gait limb ataxia, dysarthria, defects of saccadic initiation and distal weakness lower limbs. Moderate muscular wasting. Mildchoreoathetosis, Mild distal weakness upper limbs, cognitive impairment and decreased vibration sense lower limbs. Nystagmus, deep tendon reflexes lower limbs absent. APTX APTX 2 1 Sergio Piñeiro
00208954 - PubMed: Castellotti 2011 - - - - - - 0 - - EAOH Moderate gait limb ataxia, dysarthria, defects of saccadic initiation and distal weakness lower limbs and decreased vibration sense lower limbs. Mild muscular wasting. Nystagmus and deep tendon reflexes lower limbs absent. APTX APTX 2 1 Sergio Piñeiro
00208955 - PubMed: Nouri et al 2012 - - - - - - 0 - - EAOH - APTX APTX 1 1 Rick van Minkelen
00208956 15365154-Fam1 PubMed: Amouri 2004 family, 5 affected (2F, 3M), unaffacted parents F;M - Tunisia - - 0 - - EAOH ataxic gait, cerebellar ataxia, oculomotor apraxia, distal sensory disturbance, cerebellar atrophy, areflexia, distal muscle wasting, decreased motor nerve action potential, motor nerve conduction velocities and sensory action potentials APTX APTX 1 5 Rick van Minkelen
00208957 26285866-Pat23263 PubMed: van Minkelen 2015 - - - - - - 0 - - EAOH - APTX APTX 1 1 Rick van Minkelen
00208958 - - - - - - - - 0 - - EAOH - APTX APTX 1 1 Rick van Minkelen
00208959 - - - - - - - - 0 - - EAOH - APTX APTX 1 1 Rick van Minkelen
00208960 - - - - - - - - 0 - - EAOH - APTX APTX 1 1 Rick van Minkelen
00208961 - - - - - - - - 0 - - EAOH oculomotor apraxia, nystagmus (no further details given by physician) APTX APTX 1 1 Rick van Minkelen
00208962 - - - - - - - - 0 - - EAOH motoric and axonal sensible polyneuropathy, very mild dysarthria, very mild cerebellar ataxia APTX APTX 1 1 Rick van Minkelen
00208963 - van Minkelen et al. In preparation - - - - - - 0 - - EAOH cerebellar ataxia (not further details given by physician) APTX APTX 1 1 Rick van Minkelen
00208964 26285866-Pat4305 PubMed: van Minkelen 2015 - - - - - - 0 - - EAOH psychomotor retardation, epilepsy, clinically AOA1 (no details provided by requesting physician). APTX APTX 1 1 Rick van Minkelen
00208965 26285866-Pat23006 PubMed: Avan Minkelen 2015 - - - - - - 0 - - EAOH cerebellar ataxia, oculomotor apraxia (no further details given by physician) APTX APTX 1 1 Rick van Minkelen
00208966 - van Minkelen et al. In preparation - - - - - - 0 - - EAOH cerebellar ataxia (no further details given by physician) APTX APTX 1 1 Rick van Minkelen
00208967 26285866-Pat27320 PubMed: van Minkelen 2015 - - - - - - 0 - - EAOH no details given by physician APTX APTX 2 1 Rick van Minkelen
00208968 - - - - - - - - 0 - - EAOH mild AOA1 phenotype (no details provided by requesting physician) APTX APTX 1 1 Rick van Minkelen
00208969 - - - - - - - - 0 - - EAOH unknown ataxia (no further details given by physician), APTX APTX 1 1 Rick van Minkelen
00208970 - PubMed: Mosesso 2005 - - - - - - 0 - - EAOH no details provided by requesting physician APTX APTX 1 1 Rick van Minkelen
00208971 26285866-Pat27908 PubMed: Avan Minkelen 2015 - - - - - - 0 - - EAOH cerebellar ataxia, polyneuropathy, dysarthria, nystagmus, gait ataxia, mild cerebellar atrophy APTX APTX 2 1 Rick van Minkelen
00208972 - - - - - - - - 0 - - EAOH cerebellar ataxia, cerebellar dysarthria, oculomotor apraxia, legs parese iliopsoas 4+/4+, areflexia, Q10 deficiency, polyneuropathy, APTX APTX 1 1 Rick van Minkelen
00208973 - PubMed: Le Ber 2003 - - - - - - 0 - - EAOH no details provided by requesting physician APTX APTX 1 1 Rick van Minkelen
00208974 26285866-Pat1 PubMed: van Minkelen 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Morocco - - 0 - - EAOH cerebellar ataxia, cerebellar atrophy, oculomotor apraxia, ataxic gait, dysmetria, distal limb dystonia, sensitive axonal polyneuropathy, bilateral spontaneous Babinski and rotulian and achillean hyporeflexia APTX APTX 1 1 Rick van Minkelen
00208975 26285866-Pat2 PubMed: Yoon 2009, PubMed: van Minkelen 2015 2-generation family, 1affected, unaffected parents F yes Pakistan - - 0 - - EAOH oculomotor apraxia, severe dysarthria, dysmetria, bradykinesia, cerebellar atrophy, reduced deep tendon reflexes, widespread cognitive impairment APTX APTX 1 1 Rick van Minkelen
00208976 26285866-Pat18647 PubMed: Avan Minkelen 2015 - - - - - - 0 - - EAOH mild scoliosis, nystagmus, mild tremor, gait ataxia, areflexia APTX APTX 1 1 Rick van Minkelen
00208977 26285866-Pat53383 PubMed: van Minkelen 2015 - - - - - - 0 - - EAOH - APTX APTX 1 1 Rick van Minkelen
00208978 26285866-Pat62385 PubMed: van Minkelen 2015 - - - - - - 0 - - EAOH no details provided by requesting physician APTX APTX 1 1 Rick van Minkelen
00208979 26285866-Pat61291 PubMed: van Minkelen 2015 - - - - - - 0 - - EAOH no details provided by requesting physician APTX APTX 1 1 Rick van Minkelen
00208980 15365154-Fam2 PubMed: Amouri 2004 family, 4 affected (2F, 2M), unaffected parents F;M - Tunisia - - 0 - - EAOH see paper; ... APTX APTX 1 1 Johan den Dunnen
00208981 15365154-Fam3 PubMed: Amouri 2004 family, 4 affected (2F, 2M), unaffected parents F;M - Tunisia - - 0 - - EAOH see paper; ... APTX APTX 1 4 Johan den Dunnen
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