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Illnesses and symptoms treated by Genetisists in Mexico

A

Achondrogenesis Achromic Incontinentia Pigmenti Adrenomyeloneuropathy Alcaptonuria ALD Alpha-L-iduronidase Deficiency Anencephaly Apert syndrome Apolipoprotein E deficiency or defect Apolipoprotein E deficient or defective Ataxia-Telangiectasia

B

Basal Cell Nevus Syndrome

C

Cafe Au Lait Spots Café au lait spots Charcot-Marie-Tooth disease Childhood Cerebral Adrenoleukodystrophy Congenital Stationary Night Blindness Oguchi Disease Corneal Dystrophies

D

Delayed Menarche Disorders of sexual development Down syndrome Duchenne Muscular Dystrophy

E

Edwards syndrome Ehlers-Danlos Syndrome Ellis-van Creveld Syndrome

F

Familial Lipoprotein Lipase Deficiency Family History of Hearing Loss Fetal alcohol syndrome Fuchs' Dystrophy

G

Gaucher Disease Glucose-6-phosphate Dehydrogenase Deficiency

H

Hemophilia Hereditary hemorrhagic telangiectasia

I

Incontinentia Pigmenti

K

Klippel-Trenaunay-Weber syndrome

L

Lipodystrophy Lynch syndrome

M

Male infertility Mandibulofacial dysostosis Marfan syndrome Marfan's Syndrome Microcephaly Monosomy X Morquio syndrome Mullerian Anomalies Multiple Enchondromatosis Multiple Endocrine Neoplasia Multiple Endocrine Neoplasia MEN I

N

Neurofibromatosis

O

Oculocutaneous Albinism Osler-Weber-Rendu syndrome

P

Partial Androgen Insensitivity Syndrome Periodic Paralysis Syndrome Prader-Willi Syndrome Progressive peroneal neuropathic muscular atrophy Pseudohypoparathyroidism

R

Recurrent gestational loss

S

Sphingomyelinase Deficiency Spinal Muscular Atrophy SMA Steel Hair Syndrome Syndactyly

T

Thyroid cancer medullary carcinoma Turner Syndrome

V

Von Gierke Disease Von Gierke's disease