Re: type 2 test?recessive...?

[Guest guest]

In a message dated 12/29/01 6:43:00 PM, butterflypower@... writes:

<< Another question is: Is CMT type 1 and type 2 autosomal recessive,

dominant, what? >>

These are the dominant ones:

CMT & HMSN: Demyelinating

Dominant

CMT 1A: PMP-22; 17p11

CMT 1B: P0 protein; 1q22

CMT 1C: 16p13

CMT 1D: EGR2; 10q21

HNPP: PMP-22 deletion; 17p11

HMSN 3 (Dejerine-Sottas): PMP-22; P0; 8q23; EGR2

Thermosensitive

SOX10 (22q13)

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Dominant

CMT 2A: KIF1B; 1p36

CMT 2B: 3q13-q22

CMT 2C: Vocal cord D

CMT 2D: 7p14

CMT 2E: Neurofilament light chain; 8p21

CMT 2F: 7q11-q21

CMT 2G (HMSN-Proximal): 3q13.1

CMT 2-P0: P0; 1q22

HMSN 5: Pyramidal signs

HMSN 6: Eye & Ear D

HMSN + Optic atrophy

HMSN + Deafness

Ulcero-mutilation

CMT + Intermediate NCV

19p12

10q24

CMT2-P0

CMT-X (Semi-dominant)