Defective dentition

Béguez-Chédiak–Higashi syndrome (CHS) is a rare autosomal recessive disorder that arises from a mutation of a lysosomal trafficking regulator protein, which leads to a decrease in phagocytosis. The decrease in phagocytosis results in recurrent pyogenic infections, albinism, and peripheral neuropathy. [Source: Wikipedia ]

May Be Caused by
Aarskog syndrome
Aminopterin fetopathy
Apert syndrome
Bardet-Biedl syndrome
Brachmann-de Lange syndrome
Cerebro-costo-mandibular syndrome
Cherubism
Cleidocranial dysostosis
Cockayne syndrome
Coffin-Lowry syndrome
Cohen syndrome
Congenital insensitivity to pain
Cranioectodermal dysplasia
Craniometaphyseal dysplasia
Crouzon syndrome
DOOR syndrome
Dyskeratosis congenita
Dysosteosclerosis
Dysostosis Stanescu type
Ectodermal dysplasia
Ehlers-Danlos syndrome
Ellis-van Creveld syndrome
Endosteal hyperostosis Worth type
Epidermal nevus syndrome
Familial expansile osteolysis
Frontometaphyseal dysplasia
Gardner syndrome
Goltz syndrome
Gorlin syndrome
Hajdu-Cheney syndrome
Hallermann-Streiff syndrome
Hanhart syndrome
Homocystinuria
Hunter syndrome
Hurler syndrome
Hyperphosphatasia
Hypoglossia-hypodactyly
Hypomelanosis of Ito
Hypoparathyroidism
Hypophosphatasia
Hypopituitarism
Hypothyroidism
Incontinentia pigmenti
Infantile hypothyroidism
Johanson-Blizzard syndrome
KBG syndrome
Kocher-Debré-Sémélaigne syndrome
Lacrimo-auriculo-dento-digital syndrome
Lenz microphthalmia syndrome
Lenz-Majewski dysplasia
Lowe syndrome
Marinesco-Sjögren syndrome
Marshall syndrome
Melnick-Needles osteodysplasty
Mesomelic dysplasia
Morquio syndrome
Mucopolysaccharidosis
Oculo-auriculo-vertebral spectrum
Oculo-dento-osseous dysplasia
Orofaciodigital syndrome type 1
Orofaciodigital syndrome type 2
Osteogenesis imperfecta type 1
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Osteoglophonic dysplasia
Osteopetrosis
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pachyonychia congenita
Papillon-Lefèvre syndrome
Polyostotic fibrous dysplasia
Prader-Willi syndrome
Progeria
Pseudohypoparathyroidism
Pyknodysostosis
Pyle dysplasia
Rieger syndrome
Robinow syndrome
Romberg syndrome
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Sclerosteosis
Seckel syndrome
Short rib-polydactyly syndrome type 1
Singleton-Merten syndrome
Sjögren-Larsson syndrome
Stickler syndrome
Thalidomide embryopathy
Treacher Collins syndrome
Tricho-dento-osseous syndrome
Trisomy 21
Weill-Marchesani syndrome
Werner syndrome
Weyers acrodental dysostosis
Wildervanck syndrome
Williams syndrome
Winchester syndrome
XXXXY syndrome
Yunis-Varon syndrome
Aarskog syndrome
Aminopterin fetopathy
Apert syndrome
Bardet-Biedl syndrome
Brachmann-de Lange syndrome
Cerebro-costo-mandibular syndrome
Cherubism
Cleidocranial dysostosis
Cockayne syndrome
Coffin-Lowry syndrome
Cohen syndrome
Congenital insensitivity to pain
Cranioectodermal dysplasia
Craniometaphyseal dysplasia
Crouzon syndrome
DOOR syndrome
Dyskeratosis congenita
Dysosteosclerosis
Dysostosis Stanescu type
Ectodermal dysplasia
Ehlers-Danlos syndrome
Ellis-van Creveld syndrome
Endosteal hyperostosis Worth type
Epidermal nevus syndrome
Familial expansile osteolysis
Frontometaphyseal dysplasia
Gardner syndrome
Goltz syndrome
Gorlin syndrome
Hajdu-Cheney syndrome
Hallermann-Streiff syndrome
Hanhart syndrome
Homocystinuria
Hunter syndrome
Hurler syndrome
Hyperphosphatasia
Hypoglossia-hypodactyly
Hypomelanosis of Ito
Hypoparathyroidism
Hypophosphatasia
Hypopituitarism
Hypothyroidism
Incontinentia pigmenti
Infantile hypothyroidism
Johanson-Blizzard syndrome
KBG syndrome
Kocher-Debré-Sémélaigne syndrome
Lacrimo-auriculo-dento-digital syndrome
Lenz microphthalmia syndrome
Lenz-Majewski dysplasia
Lowe syndrome
Marinesco-Sjögren syndrome
Marshall syndrome
Melnick-Needles osteodysplasty
Mesomelic dysplasia
Morquio syndrome
Mucopolysaccharidosis
Oculo-auriculo-vertebral spectrum
Oculo-dento-osseous dysplasia
Orofaciodigital syndrome type 1
Orofaciodigital syndrome type 2
Osteogenesis imperfecta type 1
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Osteoglophonic dysplasia
Osteopetrosis
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pachyonychia congenita
Papillon-Lefèvre syndrome
Polyostotic fibrous dysplasia
Prader-Willi syndrome
Progeria
Pseudohypoparathyroidism
Pyknodysostosis
Pyle dysplasia
Rieger syndrome
Robinow syndrome
Romberg syndrome
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Sclerosteosis
Seckel syndrome
Short rib-polydactyly syndrome type 1
Singleton-Merten syndrome
Sjögren-Larsson syndrome
Stickler syndrome
Thalidomide embryopathy
Treacher Collins syndrome
Tricho-dento-osseous syndrome
Trisomy 21
Weill-Marchesani syndrome
Werner syndrome
Weyers acrodental dysostosis
Wildervanck syndrome
Williams syndrome
Winchester syndrome
XXXXY syndrome
Yunis-Varon syndrome